A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051742



Internal ID19140961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:38904463..39091278hg38UCSC Ensembl
Innerchr15:39196664..39383479hg19UCSC Ensembl
Innerchr15:36983956..37170771hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38186816
hg19186816
hg18186816
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2578n100
Supporting Variantsnssv3552244, nssv3552245
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051742
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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