A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3528609



Internal ID18480204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:34731652..34809429hg38UCSC Ensembl
Innerchr14:35200858..35278635hg19UCSC Ensembl
Innerchr14:34270609..34348386hg18UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg3877778
hg1977778
hg1877778
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1051540
Supporting Variants
Samples
Known GenesBAZ1A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3528609
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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