A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704437



Internal ID15441089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:98042242..98051825hg38UCSC Ensembl
Innerchr14:98508579..98518162hg19UCSC Ensembl
Innerchr14:97578332..97587915hg18UCSC Ensembl
Innerchr14:97578332..97587915hg17UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg389584
hg199584
hg189584
hg179584
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527930
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704437
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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