A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702191



Internal ID15092157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:1028355..1037340hg38UCSC Ensembl
Innerchr3:1070039..1079024hg19UCSC Ensembl
Innerchr3:1045039..1054024hg18UCSC Ensembl
Innerchr3:1045039..1054024hg17UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg388986
hg198986
hg188986
hg178986
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517343
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702191
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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