A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14034257



Internal ID4036073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:14902532..14905576hg38UCSC Ensembl
Innerchr11:14902553..14905556hg38UCSC Ensembl
Outerchr11:14902512..14905597hg38UCSC Ensembl
chr11:14924078..14927122hg19UCSC Ensembl
Innerchr11:14924099..14927102hg19UCSC Ensembl
Outerchr11:14924058..14927143hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg383045
hg193045
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625430
Supporting Variants
SamplesNA19383
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14034257
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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