A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14214329



Internal ID5009246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76961782..76966777hg38UCSC Ensembl
Innerchr11:76961818..76966742hg38UCSC Ensembl
Outerchr11:76961747..76966813hg38UCSC Ensembl
chr11:76672826..76677821hg19UCSC Ensembl
Innerchr11:76672862..76677786hg19UCSC Ensembl
Outerchr11:76672791..76677857hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg384996
hg194996
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626878
Supporting Variants
SamplesNA18507
Known GenesACER3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14214329
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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