A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041146



Internal ID19130365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:36985594..37099929hg38UCSC Ensembl
Innerchr10:37274522..37388857hg19UCSC Ensembl
Innerchr10:37314528..37428863hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38114336
hg19114336
hg18114336
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv708n100
Supporting Variantsnssv3510915
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)nsv1041146
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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