A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16984503



Internal ID57054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:69668218..69669238hg38UCSC Ensembl
chr6:70378110..70379130hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg381021
hg191021
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5458152
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16984503
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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