A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525170



Internal ID15105777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:47160140..47269724hg38UCSC Ensembl
Innerchr16:47194051..47303635hg19UCSC Ensembl
Innerchr16:45751552..45861136hg18UCSC Ensembl
Innerchr16:45751552..45861136hg17UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg38109585
hg19109585
hg18109585
hg17109585
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701244
Samples
Known GenesITFG1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525170
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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