A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042618



Internal ID19131837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20381480..20418941hg38UCSC Ensembl
Innerchr15:20586733..20624194hg19UCSC Ensembl
Innerchr15:18846747..18884208hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3837462
hg1937462
hg1837462
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2275n100
Supporting Variantsnssv3538711
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)nsv1042618
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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