A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525212



Internal ID15452505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:11436705..11451714hg38UCSC Ensembl
Innerchr10:11478704..11493713hg19UCSC Ensembl
Innerchr10:11518710..11533719hg18UCSC Ensembl
Innerchr10:11518710..11533719hg17UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3815010
hg1915010
hg1815010
hg1715010
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701294
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525212
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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