A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054921



Internal ID19144140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20336715..20418941hg38UCSC Ensembl
Innerchr15:20541968..20624194hg19UCSC Ensembl
Innerchr15:18801982..18884208hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3882227
hg1982227
hg1882227
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2247n100
Supporting Variantsnssv3536234, nssv3536236, nssv3536235
Samples
Known GenesHERC2P3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054921
Frequency
Sample Size11257
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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