A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520980



Internal ID15448273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:127582597..127617172hg38UCSC Ensembl
Innerchr10:129380861..129415436hg19UCSC Ensembl
Innerchr10:129270851..129305426hg18UCSC Ensembl
Innerchr10:129270851..129305426hg17UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3834576
hg1934576
hg1834576
hg1734576
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697720
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520980
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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