A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16986382



Internal ID58353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:109448393..109448730hg38UCSC Ensembl
chr6:109769596..109769933hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38338
hg19338
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5470030
Supporting Variants
Samples
Known GenesMICAL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16986382
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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