A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518987



Internal ID15099594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:103434329..103484808hg38UCSC Ensembl
Innerchr10:105194086..105244565hg19UCSC Ensembl
Innerchr10:105184076..105234555hg18UCSC Ensembl
Innerchr10:105184076..105234555hg17UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg3850480
hg1950480
hg1850480
hg1750480
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696455
Samples
Known GenesCALHM1, CALHM2, CALHM3, PDCD11
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518987
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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