A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698169



Internal ID15434821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:474989..495262hg38UCSC Ensembl
Innerchr5:475104..495377hg19UCSC Ensembl
Innerchr5:528104..548377hg18UCSC Ensembl
Innerchr5:528104..548377hg17UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3820274
hg1920274
hg1820274
hg1720274
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521554
Supporting Variants
Samples
Known GenesSLC9A3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698169
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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