A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701672



Internal ID15091638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:51843626..51848399hg38UCSC Ensembl
Innerchr14:52310344..52315117hg19UCSC Ensembl
Innerchr14:51380094..51384867hg18UCSC Ensembl
Innerchr14:51380094..51384867hg17UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg384774
hg194774
hg184774
hg174774
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525537
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701672
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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