A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16987606



Internal ID59178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:113624380..113658133hg38UCSC Ensembl
chr6:113945582..113979335hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3833754
hg1933754
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5454693
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16987606
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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