A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520521



Internal ID8414796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:17056936..17057017hg38UCSC Ensembl
Innerchr10:17098935..17099016hg19UCSC Ensembl
Innerchr10:17138941..17139022hg18UCSC Ensembl
Innerchr10:17138941..17139022hg17UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3882
hg1982
hg1882
hg1782
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv677604, nssv671994
Samples
Known GenesCUBN
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
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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