A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677132



Internal ID9596551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131726330..131727274hg38UCSC Ensembl
chr11:131596224..131597168hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38945
hg19945
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6445228, essv5958758, essv6527802, essv6252446, essv5475315, essv6298357, essv6066448, essv6150827, essv6463773, essv6463044, essv6027957, essv6311939, essv6416106, essv6228313, essv6267616, essv6437592, essv6254118, essv5465032, essv5953196, essv5732311, essv5557535, essv6360053, essv5963275, essv6174281, essv6569619, essv6194753, essv5904882, essv5568656, essv6306693
SamplesNA19909, NA19204, NA19377, HG01366, NA19382, NA18498, NA19904, NA19384, NA20291, NA19385, NA19172, NA19471, NA19901, NA19247, NA19455, NA19236, NA18871, NA18856, NA19099, NA19395, NA19108, NA18517, NA19435, NA20804, NA19713, NA19093, NA19213, NA19312, NA18487
Known GenesNTM
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677132
Frequency
Sample Size1151
Observed Gain0
Observed Loss29
Observed Complex0
Frequencyn/a


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