A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519699



Internal ID15100306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:29674958..29678717hg38UCSC Ensembl
Innerchr10:29963887..29967646hg19UCSC Ensembl
Innerchr10:30003893..30007652hg18UCSC Ensembl
Innerchr10:30003893..30007652hg17UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg383760
hg193760
hg183760
hg173760
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696999
Samples
Known GenesSVIL
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519699
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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