A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059718



Internal ID18802249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:82530449..82776398hg38UCSC Ensembl
Innerchr16:82564054..82810003hg19UCSC Ensembl
Innerchr16:81121555..81367504hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg38245950
hg19245950
hg18245950
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3719087
Samples
Known GenesCDH13, MIR8058
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059718
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