A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5456174



Internal ID234244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:184372736..184373375hg38UCSC Ensembl
chr4:185293890..185294529hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38640
hg19640
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16962196
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5456174
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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