A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698866



Internal ID15088832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:83618080..83622659hg38UCSC Ensembl
Innerchr16:83651685..83656264hg19UCSC Ensembl
Innerchr16:82209186..82213765hg18UCSC Ensembl
Innerchr16:82209186..82213765hg17UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg384580
hg194580
hg184580
hg174580
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523157
Supporting Variants
Samples
Known GenesCDH13
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698866
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer