A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16892351



Internal ID169096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:161007095..161007288hg38UCSC Ensembl
chr1:160976885..160977078hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38194
hg19194
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5422530
Supporting Variants
Samples
Known GenesF11R
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16892351
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.003122


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