A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040385



Internal ID18782916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101665707..101771043hg38UCSC Ensembl
Innerchr15:102205910..102311246hg19UCSC Ensembl
Innerchr15:100023433..100128769hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38105337
hg19105337
hg18105337
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2681n100
Supporting Variantsnssv3718233
Samples
Known GenesTARSL2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040385
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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