A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524966



Internal ID15105573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:103441820..103717405hg38UCSC Ensembl
Innerchr10:105201577..105477163hg19UCSC Ensembl
Innerchr10:105191567..105467153hg18UCSC Ensembl
Innerchr10:105191567..105467153hg17UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg38275586
hg19275587
hg18275587
hg17275587
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700990
Samples
Known GenesCALHM1, CALHM2, CALHM3, NEURL1, PDCD11, SH3PXD2A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524966
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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