A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5460197



Internal ID238189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:94166967..94167960hg38UCSC Ensembl
chr4:95088118..95089111hg19UCSC Ensembl
Cytoband4q22.2
Allele length
AssemblyAllele length
hg38994
hg19994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16952775
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5460197
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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