A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525452



Internal ID15106059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18714400..18780956hg38UCSC Ensembl
Innerchr11:18735947..18802503hg19UCSC Ensembl
Innerchr11:18692523..18759079hg18UCSC Ensembl
Innerchr11:18692523..18759079hg17UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3866557
hg1966557
hg1866557
hg1766557
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701580
Samples
Known GenesIGSF22, PTPN5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525452
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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