A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694930



Internal ID15084896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:46767061..46778196hg38UCSC Ensembl
Innerchr14:47236264..47247399hg19UCSC Ensembl
Innerchr14:46306014..46317149hg18UCSC Ensembl
Innerchr14:46306014..46317149hg17UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3811136
hg1911136
hg1811136
hg1711136
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517764
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694930
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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