A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16987938



Internal ID59390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110132984..110136022hg38UCSC Ensembl
chr6:110454187..110457225hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg383039
hg193039
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5466193
Supporting Variants
Samples
Known GenesWASF1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16987938
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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