A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657534



Internal ID9576953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:56087350..56089253hg38UCSC Ensembl
Outerchr19:56086979..56089623hg38UCSC Ensembl
Innerchr19:56598716..56600622hg19UCSC Ensembl
Outerchr19:56598345..56600992hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg382645
hg192648
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6362205, essv5537606, essv6419958, essv5887212, essv5643774, essv5991756, essv5970511, essv6361176, essv6554356, essv5792796, essv5693662, essv6071864, essv6278974, essv5612512, essv5516718, essv5628177, essv5396224, essv6208346, essv5928920, essv6435257, essv6376735, essv6108933, essv6328823, essv6494235, essv6488796, essv5434594, essv5635407, essv6427887, essv6115670, essv5412689, essv5615800, essv6385395, essv6155493, essv5978546, essv6479006, essv6570196, essv5564206, essv5601412, essv5410326, essv6190316, essv5699482, essv5490122, essv5826674, essv5548782, essv5843588, essv6498507, essv5900098, essv5738436, essv5842832, essv5758520, essv6243076, essv6001225, essv5472784, essv5743552, essv6430169, essv6179067, essv5995389, essv6258500, essv5755410, essv5889037, essv6087079, essv6566057, essv5916590, essv5594187, essv6142555, essv6140548, essv6266342, essv5977513, essv6206298, essv5984709, essv5540493, essv6378600, essv5626556, essv5474947, essv5432412, essv6190158, essv5946285, essv5487233, essv5496484, essv6295454, essv6306926, essv6447975, essv6222319, essv5442748, essv6247752, essv6544758
SamplesHG00626, HG00650, HG00542, HG00442, HG00592, HG00536, HG00608, HG00671, HG00524, HG00699, HG00449, HG00654, HG00693, HG00663, HG00589, HG00501, HG00702, HG00689, HG00448, HG00610, HG00537, HG00590, HG00512, HG00683, HG00534, HG00422, HG00705, HG00427, HG00530, HG00419, HG00464, HG00543, HG00560, HG00629, HG00443, HG00596, HG00557, HG00428, HG00653, HG00701, HG00657, HG00475, HG00436, HG00556, HG00584, HG00533, HG00583, HG00500, HG00619, HG00708, HG00692, HG00635, HG00651, HG00690, HG00404, HG00531, HG00479, HG00684, HG00613, HG00525, HG00704, HG00463, HG00611, HG00476, HG00625, HG00565, HG00580, HG00473, HG00607, HG00662, HG00418, HG00620, HG00707, HG00672, HG00614, HG00513, HG00578, HG00478, HG00421, HG00656, HG00698, HG00595, HG00472, HG00628, HG00437, HG00581
Known GenesZNF787
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657534
Frequency
Sample Size1151
Observed Gain0
Observed Loss86
Observed Complex0
Frequencyn/a


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