A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626157



Internal ID7012991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:44091957..44093758hg38UCSC Ensembl
Innerchr11:44091958..44093757hg38UCSC Ensembl
Outerchr11:44091956..44093759hg38UCSC Ensembl
chr11:44113507..44115308hg19UCSC Ensembl
Innerchr11:44113508..44115307hg19UCSC Ensembl
Outerchr11:44113506..44115309hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg381802
hg191802
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14116432, essv14116431, essv14116425, essv14116429, essv14116427, essv14116428, essv14116426, essv14116423, essv14116430, essv14116424
SamplesHG01066, HG01632, HG00641, HG01064, HG01510, HG02108, HG00276, HG02223, NA20334, HG00255
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626157
Frequency
Sample Size2504
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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