A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv689542



Internal ID15426194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:191926682..191950256hg38UCSC Ensembl
Innerchr3:191644471..191668045hg19UCSC Ensembl
Innerchr3:193127165..193150739hg18UCSC Ensembl
Innerchr3:193127173..193150747hg17UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3823575
hg1923575
hg1823575
hg1723575
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517535
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv689542
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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