A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694205



Internal ID15084171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:83103734..83105719hg38UCSC Ensembl
Innerchr16:83137339..83139324hg19UCSC Ensembl
Innerchr16:81694840..81696825hg18UCSC Ensembl
Innerchr16:81694840..81696825hg17UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg381986
hg191986
hg181986
hg171986
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518143
Supporting Variants
Samples
Known GenesCDH13
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694205
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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