A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16984125



Internal ID56789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:70658797..70667526hg38UCSC Ensembl
chr6:71368500..71377229hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg388730
hg198730
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5455901
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16984125
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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