A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3714616



Internal ID19012897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20380723..20525214hg38UCSC Ensembl
Innerchr15:20585976..20730453hg19UCSC Ensembl
Innerchr15:18845990..18990467hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38144492
hg19144478
hg18144478
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1053269
Supporting Variants
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)nssv3714616
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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