A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16981575



Internal ID55075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:39367529..39371878hg38UCSC Ensembl
chr6:39335305..39339654hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg384350
hg194350
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5457996
Supporting Variants
Samples
Known GenesKIF6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16981575
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000937


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