A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv671571



Internal ID15408223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:162160925..162238888hg38UCSC Ensembl
Innerchr3:161878713..161956676hg19UCSC Ensembl
Innerchr3:163361407..163439370hg18UCSC Ensembl
Innerchr3:163361415..163439378hg17UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3877964
hg1977964
hg1877964
hg1777964
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516722
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv671571
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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