A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16969868



Internal ID47227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:122639348..122665866hg38UCSC Ensembl
chr6:122960493..122987011hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3826519
hg1926519
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5465204
Supporting Variants
Samples
Known GenesPKIB
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16969868
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000625


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