A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694204



Internal ID15430856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:103315479..103317510hg38UCSC Ensembl
Innerchr14:103781816..103783847hg19UCSC Ensembl
Innerchr14:102851569..102853600hg18UCSC Ensembl
Innerchr14:102851569..102853600hg17UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg382032
hg192032
hg182032
hg172032
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518132
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694204
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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