A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694180



Internal ID15430832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:76825609..76830796hg38UCSC Ensembl
Innerchr14:77291952..77297139hg19UCSC Ensembl
Innerchr14:76361705..76366892hg18UCSC Ensembl
Innerchr14:76361705..76366892hg17UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg385188
hg195188
hg185188
hg175188
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517919
Supporting Variants
Samples
Known GenesC14orf166B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694180
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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