A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5457616



Internal ID235657
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 StatusM
Merged Variants
Supporting Variantsnssv16970085
Samples
Known GenesVNN3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5457616
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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