A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17374976



Internal ID22600645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:83661886..83664077hg38UCSC Ensembl
chr16:83695491..83697682hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg382192
hg192192
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5942303
Supporting Variants
Samples
Known GenesCDH13
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17374976
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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