A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv664676



Internal ID15054642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:8784337..8821239hg38UCSC Ensembl
Innerchr3:8826023..8862925hg19UCSC Ensembl
Innerchr3:8801023..8837925hg18UCSC Ensembl
Innerchr3:8801023..8837925hg17UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3836903
hg1936903
hg1836903
hg1736903
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517310
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv664676
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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