A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525060



Internal ID15105667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:34786889..35020439hg38UCSC Ensembl
Innerchr10:35075817..35309367hg19UCSC Ensembl
Innerchr10:35115823..35349373hg18UCSC Ensembl
Innerchr10:35115823..35349373hg17UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38233551
hg19233551
hg18233551
hg17233551
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701111
Samples
Known GenesCUL2, PARD3, PARD3-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525060
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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