A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3718149



Internal ID19016430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:85818185..85842966hg38UCSC Ensembl
Innerchr15:86361416..86386197hg19UCSC Ensembl
Innerchr15:84162420..84187201hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3824782
hg1924782
hg1824782
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1042976
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)nssv3718149
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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