A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049254



Internal ID19138473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20351177..20512131hg38UCSC Ensembl
Innerchr15:20556430..20717374hg19UCSC Ensembl
Innerchr15:18816444..18977388hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38160955
hg19160945
hg18160945
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2255n100
Supporting Variantsnssv3536343, nssv3536344
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)nsv1049254
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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