A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv667949



Internal ID15404601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:146648726..147040618hg38UCSC Ensembl
Innerchr3:146366513..146758405hg19UCSC Ensembl
Innerchr3:147849203..148241095hg18UCSC Ensembl
Innerchr3:147849211..148241103hg17UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38391893
hg19391893
hg18391893
hg17391893
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516386
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv667949
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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