A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16987733



Internal ID59265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:119016499..119016589hg38UCSC Ensembl
chr6:119337664..119337754hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5455822
Supporting Variants
Samples
Known GenesFAM184A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16987733
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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