A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519582



Internal ID15100189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5604140..5678104hg38UCSC Ensembl
Innerchr10:5646103..5720067hg19UCSC Ensembl
Innerchr10:5686109..5760073hg18UCSC Ensembl
Innerchr10:5686109..5760073hg17UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3873965
hg1973965
hg1873965
hg1773965
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv672886, nssv676923, nssv656962, nssv663512, nssv690930
Samples
Known GenesASB13
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519582
Frequency
Sample Size2026
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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