A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16985984



Internal ID58072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:55443011..55443075hg38UCSC Ensembl
chr6:55307809..55307873hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5471470
Supporting Variants
Samples
Known GenesHMGCLL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16985984
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.350902


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