A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv660175



Internal ID15396827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:48327100..48434285hg38UCSC Ensembl
Innerchr14:48796303..48903488hg19UCSC Ensembl
Innerchr14:47866053..47973238hg18UCSC Ensembl
Innerchr14:47866053..47973238hg17UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg38107186
hg19107186
hg18107186
hg17107186
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520033
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv660175
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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