A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3528599



Internal ID18480194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:34382315..34500227hg38UCSC Ensembl
Innerchr14:34851521..34969433hg19UCSC Ensembl
Innerchr14:33921272..34039184hg18UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg38117913
hg19117913
hg18117913
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050218
Supporting Variants
Samples
Known GenesSPTSSA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3528599
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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