A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559928



Internal ID18511523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:83162620..83177339hg38UCSC Ensembl
Innerchr16:83196225..83210944hg19UCSC Ensembl
Innerchr16:81753726..81768445hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3814720
hg1914720
hg1814720
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1060089
Supporting Variants
Samples
Known GenesCDH13
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3559928
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