A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16892427



Internal ID169146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:161668293..161674587hg38UCSC Ensembl
chr1:161638083..161644377hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg386295
hg196295
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138356
Supporting Variants
Samples
Known GenesFCGR2B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16892427
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.067706


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