A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051326



Internal ID19140545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20364686..20404354hg38UCSC Ensembl
Innerchr15:20569939..20609607hg19UCSC Ensembl
Innerchr15:18829953..18869621hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3839669
hg1939669
hg1839669
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2260n100
Supporting Variantsnssv3537638, nssv3537636, nssv3537637, nssv3537635
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)nsv1051326
Frequency
Sample Size11257
Observed Gain3
Observed Loss1
Observed Complex0
Frequencyn/a


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