A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv674835



Internal ID15411487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:162136930..162254709hg38UCSC Ensembl
Innerchr3:161854718..161972497hg19UCSC Ensembl
Innerchr3:163337412..163455191hg18UCSC Ensembl
Innerchr3:163337420..163455199hg17UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38117780
hg19117780
hg18117780
hg17117780
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)nssv674835
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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