A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516123



Internal ID15443416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:19031864..19056050hg38UCSC Ensembl
Innerchr10:19320793..19344979hg19UCSC Ensembl
Innerchr10:19360799..19384985hg18UCSC Ensembl
Innerchr10:19360799..19384985hg17UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3824187
hg1924187
hg1824187
hg1724187
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv676819, nssv666361
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516123
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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