A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3715554



Internal ID18667149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:23989181..24153768hg38UCSC Ensembl
Innerchr15:24234328..24398915hg19UCSC Ensembl
Innerchr15:21785421..21950008hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38164588
hg19164588
hg18164588
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1040668
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)nssv3715554
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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