A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15103231



Internal ID6033629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:94670510..94675828hg38UCSC Ensembl
Innerchr14:94670510..94675828hg38UCSC Ensembl
Outerchr14:94670010..94676328hg38UCSC Ensembl
chr14:95136847..95142165hg19UCSC Ensembl
Innerchr14:95136847..95142165hg19UCSC Ensembl
Outerchr14:95136347..95142665hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg385319
hg195319
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635386
Supporting Variants
SamplesNA19438
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15103231
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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