A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv692256



Internal ID15428908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:98711970..98727250hg38UCSC Ensembl
Innerchr14:99178307..99193587hg19UCSC Ensembl
Innerchr14:98248060..98263340hg18UCSC Ensembl
Innerchr14:98248060..98263340hg17UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3815281
hg1915281
hg1815281
hg1715281
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516436
Supporting Variants
Samples
Known GenesC14orf177
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv692256
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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