A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043536



Internal ID18786067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:45420493..45580787hg38UCSC Ensembl
Innerchr10:45915941..46076235hg19UCSC Ensembl
Innerchr10:45235947..45396241hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38160295
hg19160295
hg18160295
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3510054
Samples
Known GenesALOX5, MARCH8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043536
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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