A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5477055



Internal ID254650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:73986617..73991936hg38UCSC Ensembl
chr8:74898852..74904171hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg385320
hg195320
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17012127
Samples
Known GenesLY96
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5477055
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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