A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5460541



Internal ID238520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:178681718..179242918hg38UCSC Ensembl
chr4:179602872..180164072hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38561201
hg19561201
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16960407
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5460541
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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