A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv676336



Internal ID15066302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:103891739..103892784hg38UCSC Ensembl
Innerchr14:104358076..104359121hg19UCSC Ensembl
Innerchr14:103427829..103428874hg18UCSC Ensembl
Innerchr14:103427829..103428874hg17UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg381046
hg191046
hg181046
hg171046
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520846
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv676336
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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