A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520521



Internal ID6013844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:17098935..17099016hg19UCSC Ensembl
Innerchr10:17138941..17139022hg18UCSC Ensembl
Innerchr10:17138941..17139022hg17UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
hg17n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnssv677604, nssv671994
Samples
Known GenesCUBN
Method
AnalysisMerged-level CNV regions
PlatformIllumina HumanHap550 Genotyping BeadChip v3
Comments
ReferenceShaikh et al 2009
Pubmed ID19592680
Accession Number(s)nsv520521
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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