A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1226e199



Internal ID20124528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:100426222..100431169hg38UCSC Ensembl
chr7:100023845..100028792hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg384948
hg194948
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2672845, esv2663615
SamplesHG00626, HG00403, HG00189, HG00542, HG00536, HG00608, HG00361, HG00524, HG00187, HG00315, HG00367, HG00318, HG00181, HG00699, HG00179, HG00449, HG00177, HG00654, HG00337, HG00327, HG00271, HG00663, HG00589, HG00272, HG00501, HG00702, HG00634, HG00610, HG00346, HG00270, HG00334, HG00185, HG00537, HG00590, HG00512, HG00281, HG00277, HG00683, HG00335, HG00325, HG00705, HG00309, HG00427, HG00338, HG00326, HG00178, HG00323, HG00419, HG00464, HG00543, HG00313, HG00629, HG00443, HG00268, HG00266, HG00183, HG00176, HG00282, HG00596, HG00557, HG00328, HG00428, HG00190, HG00653, HG00577, HG00475, HG00368, HG00436, HG00556, HG00320, HG00533, HG00344, HG00275, HG00619, HG00708, HG00635, HG00324, HG00284, HG00273, HG00690, HG00404, HG00373, HG00531, HG00479, HG00331, HG00684, HG00613, HG00525, HG00321, HG00276, HG00704, HG00611, HG00476, HG00336, HG00285, HG00625, HG00353, HG00580, HG00357, HG00278, HG00473, HG00319, HG00662, HG00418, HG00620, HG00339, HG00269, HG00672, HG00614, HG00513, HG00478, HG00312, HG00329, HG00656, HG00342, HG00310, HG00186, HG00280, HG00343, HG00377, HG00274, HG00595, HG00472, HG00171, HG00437
Known GenesMEPCE, ZCWPW1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv1226e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss125
Observed Complex0
Frequencyn/a


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