A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040435



Internal ID18782966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101684138..101771043hg38UCSC Ensembl
Innerchr15:102224341..102311246hg19UCSC Ensembl
Innerchr15:100041864..100128769hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3886906
hg1986906
hg1886906
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2681n100
Supporting Variantsnssv3555401, nssv3555402, nssv3555404, nssv3555403
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)nsv1040435
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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