A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16987958



Internal ID59405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110344670..110348681hg38UCSC Ensembl
chr6:110665873..110669884hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg384012
hg194012
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5465593
Supporting Variants
Samples
Known GenesMETTL24
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16987958
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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