A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3532208



Internal ID18830489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:22159015..22509792hg38UCSC Ensembl
Innerchr14:22626948..22978775hg19UCSC Ensembl
Innerchr14:21696788..22048615hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38350778
hg19351828
hg18351828
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1041751
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)nssv3532208
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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