A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5463168



Internal ID241079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:173854695..173854879hg38UCSC Ensembl
chr4:174775846..174776030hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg38185
hg19185
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16959301
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5463168
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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