A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036658



Internal ID18779189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:24044696..24086501hg38UCSC Ensembl
Innerchr14:24513905..24555710hg19UCSC Ensembl
Innerchr14:23583745..23625550hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3841806
hg1941806
hg1841806
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3528523
Samples
Known GenesCPNE6, DHRS4L1, LRRC16B, NRL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036658
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