A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv691223



Internal ID15081189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:90502030..90559918hg38UCSC Ensembl
Innerchr14:90968374..91026262hg19UCSC Ensembl
Innerchr14:90038127..90096015hg18UCSC Ensembl
Innerchr14:90038127..90096015hg17UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg3857889
hg1957889
hg1857889
hg1757889
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)nssv691223
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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