A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528472



Internal ID15455765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:19007821..19096319hg38UCSC Ensembl
Innerchr10:19296750..19385248hg19UCSC Ensembl
Innerchr10:19336756..19425254hg18UCSC Ensembl
Innerchr10:19336756..19425254hg17UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3888499
hg1988499
hg1888499
hg1788499
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705075
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528472
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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