A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661192



Internal ID9927297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:96112149..96112814hg38UCSC Ensembl
chr15:96655378..96656043hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg38666
hg19666
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6133993, essv6314719, essv6282328, essv5634288, essv5720418, essv6532107, essv5736236, essv6104974, essv5665488, essv6289497, essv6271876, essv5888664, essv6341662, essv6359882, essv5806103, essv5989182, essv5628440, essv6533461, essv5609192, essv6020147, essv6214004, essv6247992, essv6445496, essv6373302, essv5563785, essv6162029, essv5420573, essv6374216, essv5592761
SamplesNA19700, NA12414, NA12843, HG00367, NA18545, HG00177, NA18944, NA12287, HG00270, NA19782, HG00139, NA12889, NA20342, NA19789, NA18579, HG00239, HG00250, HG01497, NA19225, NA12144, NA12716, HG00254, HG00336, NA18952, NA07037, NA12347, HG00339, HG00342, HG00171
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661192
Frequency
Sample Size1151
Observed Gain0
Observed Loss29
Observed Complex0
Frequencyn/a


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