A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5896121



Internal ID22671210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:124473153..124478755hg38UCSC Ensembl
chr4:125394308..125399910hg19UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg385603
hg195603
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17414340
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5896121
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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