A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1158e199



Internal ID22758931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:142943308..142947655hg38UCSC Ensembl
chr6:143264445..143268792hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg384348
hg194348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2667220, esv2674945
SamplesHG00626, HG00403, HG01441, HG00650, HG00442, HG01356, HG00536, HG00608, HG00671, HG00361, HG00524, HG01389, HG01374, HG00315, HG00318, HG00181, HG01465, HG00699, HG00179, HG00449, HG00654, HG01140, HG00693, HG00337, HG00327, HG00271, HG00663, HG01350, HG01366, HG00589, HG00272, HG00501, HG01351, HG00702, HG00689, HG00448, HG00330, HG00634, HG00610, HG00346, HG01354, HG00369, HG00270, HG01365, HG00334, HG00185, HG00537, HG00590, HG01134, HG00512, HG00281, HG00277, HG00683, HG00335, HG00325, HG00534, HG00422, HG00705, HG01440, HG00309, HG00182, HG00427, HG00338, HG00326, HG00178, HG00323, HG00530, HG00419, HG00464, HG01353, HG00543, HG00313, HG01136, HG00443, HG00268, HG00266, HG00183, HG00282, HG00596, HG01384, HG00557, HG00328, HG00428, HG00653, HG00701, HG00657, HG00475, HG00368, HG00436, HG00556, HG00320, HG00584, HG00533, HG00583, HG00344, HG01498, HG00500, HG00275, HG00619, HG00708, HG00692, HG00635, HG01390, HG00324, HG00284, HG00273, HG00651, HG00690, HG00404, HG00373, HG00531, HG00479, HG00331, HG00684, HG01383, HG00613, HG00525, HG00321, HG00276, HG00704, HG00463, HG01148, HG00611, HG00476, HG00336, HG00285, HG00625, HG00366, HG00353, HG00580, HG00375, HG00357, HG00278, HG01357, HG01375, HG00473, HG00607, HG00319, HG00662, HG00418, HG01489, HG00620, HG00339, HG00269, HG00707, HG00672, HG00614, HG00513, HG00578, HG00478, HG01491, HG00421, HG00329, HG00656, HG00342, HG00310, HG00186, HG00698, HG00280, HG00343, HG00377, HG00372, HG00274, HG00595, HG00472, HG00628, HG00345, HG00437, HG00581
Known GenesHIVEP2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv1158e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss169
Observed Complex0
Frequencyn/a


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