A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3713493



Internal ID19011774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:49056219..49355999hg38UCSC Ensembl
Innerchr14:49522937..49822717hg19UCSC Ensembl
Innerchr14:48592687..48892467hg18UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg38299781
hg19299781
hg18299781
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1037038
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)nssv3713493
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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