A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5899729



Internal ID22674862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:79777114..79784749hg38UCSC Ensembl
chr4:80698268..80705903hg19UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg387636
hg197636
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17413241
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5899729
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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