A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3530146



Internal ID18828427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:40466959..40741799hg38UCSC Ensembl
Innerchr14:40936163..41211004hg19UCSC Ensembl
Innerchr14:40005913..40280754hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38274841
hg19274842
hg18274842
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1054806
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)nssv3530146
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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