A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520890



Internal ID15448183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:18505299..18506268hg38UCSC Ensembl
Innerchr2:18686565..18687534hg19UCSC Ensembl
Innerchr2:18550046..18551015hg18UCSC Ensembl
Innerchr2:18608193..18609162hg17UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg38970
hg19970
hg18970
hg17970
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv677239, nssv689398, nssv677023, nssv689757
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520890
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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