A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16980772



Internal ID54551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:22166500..22176000hg38UCSC Ensembl
chr6:22166729..22176229hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg389501
hg199501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5468764
Supporting Variants
Samples
Known GenesCASC15
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16980772
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.049656


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