A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5897383



Internal ID22672485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:79776653..79779077hg38UCSC Ensembl
chr4:80697807..80700231hg19UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg382425
hg192425
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17425725
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5897383
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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