A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699187



Internal ID15435839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:86961298..87051850hg38UCSC Ensembl
Innerchr14:87427642..87518194hg19UCSC Ensembl
Innerchr14:86497395..86587947hg18UCSC Ensembl
Innerchr14:86497395..86587947hg17UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3890553
hg1990553
hg1890553
hg1790553
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523432
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699187
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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