A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16983387



Internal ID56300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:57236000..57268000hg38UCSC Ensembl
chr6:57100798..57132798hg19UCSC Ensembl
Cytoband6p11.2
Allele length
AssemblyAllele length
hg3832001
hg1932001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5464263
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16983387
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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