A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17710335



Internal ID134001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87934498..87946128hg38UCSC Ensembl
chr16:87968104..87979734hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3811631
hg1911631
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5526311
Supporting Variants
Samples
Known GenesCA5A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17710335
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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