A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16986381



Internal ID58352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:109446850..109447147hg38UCSC Ensembl
chr6:109768053..109768350hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38298
hg19298
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5456755
Supporting Variants
Samples
Known GenesMICAL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16986381
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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