A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3716724



Internal ID19015005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:52698270..52738406hg38UCSC Ensembl
Innerchr15:52990467..53030603hg19UCSC Ensembl
Innerchr15:50777759..50817895hg18UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3840137
hg1940137
hg1840137
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1049055
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)nssv3716724
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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