A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054379



Internal ID19143598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20372787..20530173hg38UCSC Ensembl
Innerchr15:20578040..20735411hg19UCSC Ensembl
Innerchr15:18838054..18995425hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38157387
hg19157372
hg18157372
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2256n100
Supporting Variantsnssv3535831, nssv3535832
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)nsv1054379
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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