A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3712159



Internal ID18663754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:21988852..22509792hg38UCSC Ensembl
Innerchr14:22457092..22978775hg19UCSC Ensembl
Innerchr14:21526932..22048615hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38520941
hg19521684
hg18521684
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036343
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)nssv3712159
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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