A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5464174



Internal ID242054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:74351177..74424152hg38UCSC Ensembl
chr6:75060893..75133868hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3872976
hg1972976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16987267
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5464174
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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