A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17704748



Internal ID128414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:20767235..20767539hg38UCSC Ensembl
chr16:20778557..20778861hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5515318
Supporting Variants
Samples
Known GenesACSM3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17704748
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.603125


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