A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3713487



Internal ID19011768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:48193242..48242035hg38UCSC Ensembl
Innerchr14:48662445..48711238hg19UCSC Ensembl
Innerchr14:47732195..47780988hg18UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3848794
hg1948794
hg1848794
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1042690
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)nssv3713487
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer