A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040436



Internal ID19129655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:62515778..62568827hg38UCSC Ensembl
Innerchr15:62807977..62861026hg19UCSC Ensembl
Innerchr15:60595269..60648318hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3853050
hg1953050
hg1853050
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3717950
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)nsv1040436
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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