A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677074



Internal ID9943179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:61650116..61681475hg38UCSC Ensembl
chr9:44857954..44889313hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3831360
hg1931360
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6129605, essv5626955, essv6050216, essv5635141, essv5599729, essv5632607, essv5643991, essv6231542, essv5693085, essv5867330, essv5813419, essv6582667, essv5605811, essv6134967, essv6396548, essv5907468, essv5931677, essv6344948, essv5807401, essv6176900, essv5747986, essv6185582, essv6507102, essv6398461, essv5932749, essv5468774, essv6170751, essv6219532, essv6579262, essv5443967, essv5623384, essv6243634, essv6258398, essv5541964, essv6393448, essv5876028, essv6031246
SamplesHG00114, NA19909, NA19684, HG00737, NA19381, NA18550, NA19062, NA19404, NA19651, NA18977, NA19235, NA19722, HG01048, NA20533, NA18867, NA19007, NA19908, NA19070, NA19670, HG00145, HG01384, NA19403, NA18910, NA18553, NA19625, NA18541, NA19375, HG00638, NA20778, NA19311, NA19083, NA19360, NA19376, HG01491, HG01378, NA19312, NA18577
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677074
Frequency
Sample Size1151
Observed Gain0
Observed Loss37
Observed Complex0
Frequencyn/a


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