A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698834



Internal ID15088800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161681274..161685552hg38UCSC Ensembl
Innerchr1:161651064..161655342hg19UCSC Ensembl
Innerchr1:159917688..159921966hg18UCSC Ensembl
Innerchr1:158382729..158387000hg17UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg384279
hg194279
hg184279
hg174272
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517640
Supporting Variants
Samples
Known GenesRPL31P11
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698834
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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