A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16981569



Internal ID55072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:39337529..39339735hg38UCSC Ensembl
chr6:39305305..39307511hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg382207
hg192207
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5466734
Supporting Variants
Samples
Known GenesKIF6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16981569
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000624


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