A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3681688



Internal ID18979969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:8703686..8755877hg38UCSC Ensembl
Innerchr8:8561196..8613387hg19UCSC Ensembl
Innerchr8:8598606..8650797hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3852192
hg1952192
hg1852192
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1022670
Supporting Variants
Samples
Known GenesCLDN23
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3681688
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