A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520311



Internal ID15447604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:26534116..26535012hg38UCSC Ensembl
Innerchr10:26823045..26823941hg19UCSC Ensembl
Innerchr10:26863051..26863947hg18UCSC Ensembl
Innerchr10:26863051..26863947hg17UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38897
hg19897
hg18897
hg17897
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697340
Samples
Known GenesAPBB1IP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520311
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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