A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16969823



Internal ID47199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:134376230..134376306hg38UCSC Ensembl
chr6:134697368..134697444hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5454635
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16969823
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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