A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520736



Internal ID15448029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:20342484..20573498hg38UCSC Ensembl
Innerchr10:20631413..20862427hg19UCSC Ensembl
Innerchr10:20671419..20902433hg18UCSC Ensembl
Innerchr10:20671419..20902433hg17UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38231015
hg19231015
hg18231015
hg17231015
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697582
Samples
Known GenesMIR4675
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520736
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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