A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3531041



Internal ID18829322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:57938806..57976653hg38UCSC Ensembl
Innerchr14:58405524..58443371hg19UCSC Ensembl
Innerchr14:57475277..57513124hg18UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg3837848
hg1937848
hg1837848
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052712
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)nssv3531041
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