A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3530226



Internal ID18828507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:43275491..43695153hg38UCSC Ensembl
Innerchr14:43744694..44164356hg19UCSC Ensembl
Innerchr14:42814444..43234106hg18UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38419663
hg19419663
hg18419663
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1040702
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)nssv3530226
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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