A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5893018



Internal ID22668075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:82339125..82339190hg38UCSC Ensembl
chr4:83260278..83260343hg19UCSC Ensembl
Cytoband4q21.22
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17418575
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5893018
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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