A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16986020



Internal ID58100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:55690000..55741500hg38UCSC Ensembl
chr6:55554798..55606298hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3851501
hg1951501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5459213
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16986020
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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