A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662466



Internal ID9928571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:703716..708522hg38UCSC Ensembl
Outerchr19:703345..708892hg38UCSC Ensembl
Innerchr19:703716..708522hg19UCSC Ensembl
Outerchr19:703345..708892hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg385548
hg195548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6375264, essv6209383, essv5770150, essv6496767, essv6383697, essv6566204, essv6246820, essv6052959, essv5768867, essv6013232, essv6488221, essv5436669, essv6109949, essv5855593, essv5980781, essv6477740, essv6427409, essv6155554, essv6379891, essv5918775, essv5896147, essv6269014, essv6275723, essv6263511, essv5997596, essv5565210, essv5614748, essv6201404, essv6336002, essv6390763, essv6387900, essv5511241, essv6380225, essv6157593, essv5677999, essv5510965, essv6561136, essv6545180, essv6450633, essv5564505, essv5837789, essv6001294, essv6465973, essv6534416, essv6559490, essv6482565, essv5832118
SamplesHG00626, HG00403, HG00650, HG00542, HG00536, HG00524, HG00566, HG00663, HG00501, HG00689, HG00634, HG00610, HG00590, HG00512, HG00705, HG00530, HG00419, HG00464, HG00629, HG00596, HG00557, HG00428, HG00653, HG00556, HG00533, HG00583, HG00500, HG00708, HG00690, HG00404, HG00613, HG00525, HG00704, HG00611, HG00476, HG00565, HG00580, HG00473, HG00607, HG00418, HG00614, HG00513, HG00578, HG00478, HG00656, HG00595, HG00628
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662466
Frequency
Sample Size1151
Observed Gain0
Observed Loss47
Observed Complex0
Frequencyn/a


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