A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3712292



Internal ID19010573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:40049637..40137182hg38UCSC Ensembl
Innerchr14:40518841..40606386hg19UCSC Ensembl
Innerchr14:39588592..39676137hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3887546
hg1987546
hg1887546
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1037101
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)nssv3712292
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