A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv672759



Internal ID15409411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:35340038..35369183hg38UCSC Ensembl
Innerchr14:35809244..35838389hg19UCSC Ensembl
Innerchr14:34878995..34908140hg18UCSC Ensembl
Innerchr14:34878995..34908140hg17UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg3829146
hg1929146
hg1829146
hg1729146
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518090
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv672759
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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