A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515889



Internal ID15096496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:72072821..72077662hg38UCSC Ensembl
Innerchr10:73832579..73837420hg19UCSC Ensembl
Innerchr10:73502585..73507426hg18UCSC Ensembl
Innerchr10:73502585..73507426hg17UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg384842
hg194842
hg184842
hg174842
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv665162, nssv683854
Samples
Known GenesSPOCK2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515889
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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