A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv691749



Internal ID15081715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:90511511..90560888hg38UCSC Ensembl
Innerchr14:90977855..91027232hg19UCSC Ensembl
Innerchr14:90047608..90096985hg18UCSC Ensembl
Innerchr14:90047608..90096985hg17UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg3849378
hg1949378
hg1849378
hg1749378
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520068
Supporting Variants
Samples
Known GenesTTC7B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv691749
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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