A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625437



Internal ID7012271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:15508231..15515046hg38UCSC Ensembl
Innerchr11:15508231..15515046hg38UCSC Ensembl
Outerchr11:15507960..15515302hg38UCSC Ensembl
chr11:15529777..15536592hg19UCSC Ensembl
Innerchr11:15529777..15536592hg19UCSC Ensembl
Outerchr11:15529506..15536848hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg386816
hg196816
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14034664, essv14034662, essv14034663
SamplesHG02360, HG00436, HG01872
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625437
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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