A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035386



Internal ID19124605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:44206707..44384976hg38UCSC Ensembl
Innerchr15:44498905..44677174hg19UCSC Ensembl
Innerchr15:42286197..42464466hg18UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg38178270
hg19178270
hg18178270
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2587n100
Supporting Variantsnssv3552337
Samples
Known GenesCASC4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035386
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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