A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3555229



Internal ID18853510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:92336614..92367076hg38UCSC Ensembl
Innerchr15:92879844..92910306hg19UCSC Ensembl
Innerchr15:90680848..90711310hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3830463
hg1930463
hg1830463
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1041582
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)nssv3555229
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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