A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5998592



Internal ID21907935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:76423158..76423391hg38UCSC Ensembl
chr4:77344311..77344544hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg38234
hg19234
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17544082
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5998592
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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