A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5893918



Internal ID22668986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:79645407..79686403hg38UCSC Ensembl
chr4:80566561..80607557hg19UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg3840997
hg1940997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17428396
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5893918
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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