A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031377



Internal ID18773911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:19289979..20971814hg38UCSC Ensembl
Innerchr5:19290088..20971923hg19UCSC Ensembl
Innerchr5:19325845..21007680hg18UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg381681836
hg191681836
hg181681836
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3635908
Samples
Known GenesCDH18
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1031377
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