A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5469130



Internal ID246921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:164324963..164340952hg38UCSC Ensembl
chr6:164745996..164761985hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3815990
hg1915990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16990565
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5469130
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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