A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16979408



Internal ID53646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:28082157..28082337hg38UCSC Ensembl
chr6:28049935..28050115hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38181
hg19181
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5470660
Supporting Variants
Samples
Known GenesZNF165
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16979408
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.004059


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