A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625430



Internal ID6665577
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14034257, essv14034255, essv14034256, essv14034258, essv14034259
SamplesNA19404, NA19383, HG01077, NA19452, NA19030
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625430
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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