A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054640



Internal ID19143859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20380723..20530173hg38UCSC Ensembl
Innerchr15:20585976..20735411hg19UCSC Ensembl
Innerchr15:18845990..18995425hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38149451
hg19149436
hg18149436
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2243n100
Supporting Variantsnssv3714619, nssv3714621, nssv3714622, nssv3537210, nssv3714618, nssv3714620
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)nsv1054640
Frequency
Sample Size11257
Observed Gain2
Observed Loss4
Observed Complex0
Frequencyn/a


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