A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040966



Internal ID18783497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:2650087..3044294hg38UCSC Ensembl
Innerchr10:2692279..3086486hg19UCSC Ensembl
Innerchr10:2682279..3076486hg18UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg38394208
hg19394208
hg18394208
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv660n100
Supporting Variantsnssv3486677
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040966
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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