A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039237



Internal ID18781768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101684138..101766295hg38UCSC Ensembl
Innerchr15:102224341..102306498hg19UCSC Ensembl
Innerchr15:100041864..100124021hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3882158
hg1982158
hg1882158
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2681n100
Supporting Variantsnssv3555400
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)nsv1039237
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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