A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15036750



Internal ID3807512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:62177774..62212062hg38UCSC Ensembl
Innerchr14:62177803..62212034hg38UCSC Ensembl
Outerchr14:62177746..62212091hg38UCSC Ensembl
chr14:62644492..62678780hg19UCSC Ensembl
Innerchr14:62644521..62678752hg19UCSC Ensembl
Outerchr14:62644464..62678809hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg3834289
hg1934289
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3634704
Supporting Variants
SamplesHG03451
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15036750
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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