A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv670349



Internal ID15407001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:21215817..21304147hg38UCSC Ensembl
Innerchr3:21257309..21345639hg19UCSC Ensembl
Innerchr3:21232313..21320643hg18UCSC Ensembl
Innerchr3:21232313..21320643hg17UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3888331
hg1988331
hg1888331
hg1788331
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516562
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv670349
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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