A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696827



Internal ID15433479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:46132889..46138696hg38UCSC Ensembl
Innerchr14:46602092..46607899hg19UCSC Ensembl
Innerchr14:45671842..45677649hg18UCSC Ensembl
Innerchr14:45671842..45677649hg17UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg385808
hg195808
hg185808
hg175808
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516946
Supporting Variants
Samples
Known GenesLINC00871
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696827
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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