A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696515



Internal ID15433167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:101378772..101382374hg38UCSC Ensembl
Innerchr14:101845109..101848711hg19UCSC Ensembl
Innerchr14:100914862..100918464hg18UCSC Ensembl
Innerchr14:100914862..100918464hg17UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg383603
hg193603
hg183603
hg173603
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517359
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696515
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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