A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5451998



Internal ID230162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1515519..1518686hg38UCSC Ensembl
chr4:1517246..1520413hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg383168
hg193168
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16945642
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5451998
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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