A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050575



Internal ID18793106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:68482000..68554748hg38UCSC Ensembl
Innerchr15:68774339..68847087hg19UCSC Ensembl
Innerchr15:66561393..66634141hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3872749
hg1972749
hg1872749
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3717957
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)nsv1050575
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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