A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16970085



Internal ID47382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:132734103..132740731hg38UCSC Ensembl
chr6:133055242..133061870hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg386629
hg196629
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5457616
Supporting Variants
Samples
Known GenesVNN3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16970085
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001093


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