A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14103192



Internal ID4050264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:39960729..39967272hg38UCSC Ensembl
Innerchr11:39960778..39967224hg38UCSC Ensembl
Outerchr11:39960681..39967321hg38UCSC Ensembl
chr11:39982279..39988822hg19UCSC Ensembl
Innerchr11:39982328..39988774hg19UCSC Ensembl
Outerchr11:39982231..39988871hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg386544
hg196544
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626054
Supporting Variants
SamplesHG03693
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14103192
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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