A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14210772



Internal ID4367936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:72141339..72179940hg38UCSC Ensembl
Innerchr11:72141489..72179790hg38UCSC Ensembl
Outerchr11:72141189..72180090hg38UCSC Ensembl
chr11:71852383..71890984hg19UCSC Ensembl
Innerchr11:71852533..71890834hg19UCSC Ensembl
Outerchr11:71852233..71891134hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3838602
hg1938602
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626792
Supporting Variants
SamplesHG03898
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14210772
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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