A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022665



Internal ID19111883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:24560072..24578029hg38UCSC Ensembl
Innerchr5:24560181..24578138hg19UCSC Ensembl
Innerchr5:24595938..24613895hg18UCSC Ensembl
Cytoband5p14.2
Allele length
AssemblyAllele length
hg3817958
hg1917958
hg1817958
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3635949
Samples
Known GenesCDH10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022665
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