A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635525



Internal ID7022324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:101211536..101216103hg38UCSC Ensembl
Innerchr14:101211578..101216062hg38UCSC Ensembl
Outerchr14:101211495..101216145hg38UCSC Ensembl
chr14:101677873..101682440hg19UCSC Ensembl
Innerchr14:101677915..101682399hg19UCSC Ensembl
Outerchr14:101677832..101682482hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg384568
hg194568
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15108805
SamplesHG03899
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635525
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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