A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5900963



Internal ID22676110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:63585802..64235505hg38UCSC Ensembl
chr4:64451520..65101223hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg38649704
hg19649704
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17426001
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5900963
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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