A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695814



Internal ID15085780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:75815818..75849722hg38UCSC Ensembl
Innerchr14:76282161..76316065hg19UCSC Ensembl
Innerchr14:75351914..75385818hg18UCSC Ensembl
Innerchr14:75351914..75385818hg17UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3833905
hg1933905
hg1833905
hg1733905
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518383
Supporting Variants
Samples
Known GenesTTLL5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695814
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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