A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702268



Internal ID15438920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:45989493..46026758hg38UCSC Ensembl
Innerchr14:46458696..46495961hg19UCSC Ensembl
Innerchr14:45528446..45565711hg18UCSC Ensembl
Innerchr14:45528446..45565711hg17UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg3837266
hg1937266
hg1837266
hg1737266
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516946
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702268
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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