A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041382



Internal ID19130601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:87109614..87133963hg38UCSC Ensembl
Innerchr15:87652845..87677194hg19UCSC Ensembl
Innerchr15:85453849..85478198hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3824350
hg1924350
hg1824350
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3555099
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)nsv1041382
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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