A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038835



Internal ID18781366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101491141..101771043hg38UCSC Ensembl
Innerchr15:102031344..102311246hg19UCSC Ensembl
Innerchr15:99848867..100128769hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38279903
hg19279903
hg18279903
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2675n100
Supporting Variantsnssv3555364, nssv3555363, nssv3555362
Samples
Known GenesTARSL2, TM2D3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038835
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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