A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050701



Internal ID19139920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20327352..20411461hg38UCSC Ensembl
Innerchr15:20532605..20616714hg19UCSC Ensembl
Innerchr15:18792619..18876728hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3884110
hg1984110
hg1884110
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2242n100
Supporting Variantsnssv3536142, nssv3536144, nssv3536143
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)nsv1050701
Frequency
Sample Size11257
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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