A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5469788



Internal ID247564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:28089450..28089512hg38UCSC Ensembl
chr6:28057228..28057290hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16979409
Samples
Known GenesZNF165
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5469788
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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