A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050693



Internal ID18793224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101685418..101771043hg38UCSC Ensembl
Innerchr15:102225621..102311246hg19UCSC Ensembl
Innerchr15:100043144..100128769hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3885626
hg1985626
hg1885626
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2681n100
Supporting Variantsnssv3718236
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)nsv1050693
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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