A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525869



Internal ID15453162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:178401581..178436727hg38UCSC Ensembl
Innerchr3:178119369..178154515hg19UCSC Ensembl
Innerchr3:179602063..179637209hg18UCSC Ensembl
Innerchr3:179602071..179637217hg17UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3835147
hg1935147
hg1835147
hg1735147
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702069
Samples
Known GenesLINC01014
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525869
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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