A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043018



Internal ID19132237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:20463613..20495307hg38UCSC Ensembl
Innerchr10:20752542..20784236hg19UCSC Ensembl
Innerchr10:20792548..20824242hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3831695
hg1931695
hg1831695
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3514706
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)nsv1043018
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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