A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3555234



Internal ID18506829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:93033752..93055210hg38UCSC Ensembl
Innerchr15:93576982..93598440hg19UCSC Ensembl
Innerchr15:91377986..91399444hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3821459
hg1921459
hg1821459
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1045427
Supporting Variants
Samples
Known GenesRGMA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3555234
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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