A curated catalogue of human genomic structural variation

Variant Details

Variant: dgv26e199

Internal ID18982080
Location Information
TypeCoordinatesAssemblyOther Links
chr1:19434933..19435099hg38UCSC Ensembl
chr1:19761427..19761593hg19UCSC Ensembl
Allele length
AssemblyAllele length
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2673483, esv2666198
SamplesHG00323, HG00613, NA11881, NA12827, NA18621, HG00309, HG00313, NA19445, HG01518, NA18861, HG00252, HG00257, NA18520, NA18595, HG00182, NA20278, HG00619, HG01250, NA18534, HG01052, NA12286, HG01075, NA18561, NA18933, HG00127, HG00328, NA20752, NA18975, NA19114, HG00437, HG00500, NA11920, HG00369, HG01083, NA18612, HG00274, HG00186, NA18501, NA10847, NA19319, NA18948, NA19670, NA19331, HG01082, NA18953, NA18972, NA12828, NA18517, NA20529, HG00542, HG01174, NA19449, HG00326, HG01491, NA18608, NA18541, NA19210, HG00701, NA12058, NA18507, HG00683, HG00334, HG00187, NA20314, NA19004, HG00280, HG00557, HG00177, NA18965, HG00319, HG00737, HG00699, NA18557, NA12044, NA19467, HG01551, NA18943, HG00353, NA18596, NA20586, HG00554, HG01133, HG01521, NA18632, HG00244, HG00266, NA12414, HG00154, NA18559, HG00339, NA19428, HG00242, NA12763, HG00346, HG00250, HG01140, NA19239, HG00593, HG00583, NA12004, HG00337, HG00140, NA18622, NA18960, HG00180, HG00259, NA07357, NA18623, NA20504, HG01048, HG00231, HG00372, HG00692, NA18636, HG01124, NA19083, NA19088, HG00330, NA12761, NA18956, HG00338, NA20541, NA18609, HG00419, NA18547, HG00125, HG01360, NA12829, HG01113, NA11894, NA20520, NA19773, HG00174, HG00634, HG00254, NA19663, HG00276, NA12830, HG00237, HG00343, NA12144, HG00584, NA19316, HG00662, NA19728, NA20773, HG00620, NA19313, NA12046, HG00108, NA18620, HG01465, NA18633, HG00653, NA18572, HG00268, NA18486, NA12275, HG00260, NA18558, NA19664, HG00501, HG00273, HG00282, HG00232, HG00478, NA18942, NA18961, HG00740, HG00524, HG00512, HG00534, HG00246, HG00525, NA12283, NA19328, HG00377, NA19789, NA18945, NA18606, NA19777, HG00120, NA18940, NA12891, NA18987, NA10851, NA18582, HG01137, NA18597, NA18983, HG00443, NA18599, NA18909, NA18567, NA12749, HG00650, NA19394, NA18565, NA19009, NA12156, NA19116, HG00448, NA18602, NA18577, HG00654, NA20507, NA18548, NA11830, NA12003, NA19749, HG00285, NA11993, HG00656, NA19160, HG01366, NA19732, HG00367, NA12045, NA11932, NA18611, HG01125, HG00251, HG00275, HG00324, HG00690, NA18853, HG00183, HG01374, HG00473, HG01522, NA19381, NA20524, HG00684, HG01377, HG00336, HG00476, NA19087, HG00345, HG00278, NA18519, NA19466, NA18980, HG01067, HG00361
Known GenesCAPZB
AnalysisNo reference, merging analysis
Pubmed ID23128226
Accession Number(s)dgv26e199
Sample Size1151
Observed Gain0
Observed Loss244
Observed Complex0

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