A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14034663



Internal ID2050461
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625437
Supporting Variants
SamplesHG01872
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14034663
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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