A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3712273



Internal ID19010554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:27442502..27555238hg38UCSC Ensembl
Innerchr14:27911708..28024444hg19UCSC Ensembl
Innerchr14:26981548..27094284hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38112737
hg19112737
hg18112737
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1040926
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)nssv3712273
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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