A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3531013



Internal ID18829294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:48952406..49018981hg38UCSC Ensembl
Innerchr14:49421609..49488184hg19UCSC Ensembl
Innerchr14:48491359..48557934hg18UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3866576
hg1966576
hg1866576
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1042896
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)nssv3531013
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