A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3552366



Internal ID18850647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:45916829..46061687hg38UCSC Ensembl
Innerchr15:46209027..46353885hg19UCSC Ensembl
Innerchr15:43996319..44141177hg18UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38144859
hg19144859
hg18144859
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1046789
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3552366
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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