A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036069



Internal ID18778600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:103398289..103457152hg38UCSC Ensembl
Innerchr10:105158046..105216909hg19UCSC Ensembl
Innerchr10:105148036..105206899hg18UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg3858864
hg1958864
hg1858864
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv965n100
Supporting Variantsnssv3706210, nssv3706211, nssv3504887
Samples
Known GenesCALHM1, CALHM2, PDCD11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036069
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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