A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5537743



Internal ID312976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:154924493..154924530hg38UCSC Ensembl
chr4:155845645..155845682hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16957187
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5537743
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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