A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050632



Internal ID19139851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20380723..20411461hg38UCSC Ensembl
Innerchr15:20585976..20616714hg19UCSC Ensembl
Innerchr15:18845990..18876728hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3830739
hg1930739
hg1830739
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2271n100
Supporting Variantsnssv3537139, nssv3536026, nssv3536028, nssv3536027, nssv3537138, nssv3714591, nssv3536029, nssv3537137, nssv3536025
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)nsv1050632
Frequency
Sample Size11257
Observed Gain3
Observed Loss6
Observed Complex0
Frequencyn/a


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