A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701024



Internal ID15090990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:160315..179398hg38UCSC Ensembl
Innerchr3:201998..221081hg19UCSC Ensembl
Innerchr3:176998..196081hg18UCSC Ensembl
Innerchr3:176998..196081hg17UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3819084
hg1919084
hg1819084
hg1719084
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521040
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701024
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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