A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528622



Internal ID15109229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:71231338..71231628hg38UCSC Ensembl
Innerchr10:72991095..72991385hg19UCSC Ensembl
Innerchr10:72661101..72661391hg18UCSC Ensembl
Innerchr10:72661101..72661391hg17UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38291
hg19291
hg18291
hg17291
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705252
Samples
Known GenesUNC5B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528622
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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