A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045486



Internal ID19134705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:57340817..57494394hg38UCSC Ensembl
Innerchr15:57633015..57786592hg19UCSC Ensembl
Innerchr15:55420307..55573884hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38153578
hg19153578
hg18153578
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2607n100
Supporting Variantsnssv3553587
Samples
Known GenesCGNL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045486
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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