A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16991107



Internal ID61478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:160897949..160898603hg38UCSC Ensembl
chr6:161318981..161319635hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38655
hg19655
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5472142
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16991107
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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