A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515622



Internal ID15443233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:54090274..54096099hg38UCSC Ensembl
Innerchr13:54664409..54670234hg19UCSC Ensembl
Innerchr13:53562410..53568235hg18UCSC Ensembl
Innerchr13:53562410..53568235hg17UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg385826
hg195826
hg185826
hg175826
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv688520, nssv677914
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515622
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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