A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516860



Internal ID15097467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:100198475..100246924hg38UCSC Ensembl
Innerchr10:101958232..102006681hg19UCSC Ensembl
Innerchr10:101948222..101996671hg18UCSC Ensembl
Innerchr10:101948222..101996671hg17UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg3848450
hg1948450
hg1848450
hg1748450
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv687282, nssv654515
Samples
Known GenesCHUK, CWF19L1, SNORA12
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516860
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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