A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670359



Internal ID9936464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:99723812..99724314hg38UCSC Ensembl
chr15:100264017..100264519hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38503
hg19503
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6225078, essv6086604, essv6459230, essv5719320, essv6282899, essv6147373, essv6457863, essv6404282, essv6512867, essv6208872, essv5790605, essv5650098, essv6439867, essv5869727, essv5774238, essv5632143, essv6315344, essv5880758, essv6392647, essv5659608, essv6048378, essv5576190, essv6450625, essv6052860, essv6557927, essv5852346, essv6393196, essv5767246, essv6406027, essv5806069, essv5858750, essv6396235, essv6031242, essv6552422, essv5665666, essv6285728, essv6478219, essv6336087, essv6147651, essv6000002, essv5951405, essv5551463, essv6131617, essv5468074, essv6337902, essv5425314, essv5954832, essv5572859, essv6040521, essv6152386
SamplesNA18502, NA19909, NA19204, NA19359, NA18870, NA19107, NA19382, NA19916, NA11992, NA19138, NA20291, HG01110, HG01440, NA19189, NA19239, NA20127, NA19451, NA19247, NA19707, NA19462, NA18516, NA19982, NA18910, NA18871, HG01047, NA18912, NA19452, NA19469, NA19318, HG01107, HG01075, NA19147, NA18564, NA19435, NA19240, NA19380, NA19439, NA19470, NA19428, NA19360, NA19398, NA19248, NA19472, NA19468, NA19093, NA18873, NA18505, NA18488, NA18522, HG00554
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670359
Frequency
Sample Size1151
Observed Gain0
Observed Loss50
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer