A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5898728



Internal ID22673848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:113733969..113845758hg38UCSC Ensembl
chr5:113069666..113181455hg19UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg38111790
hg19111790
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17412845
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5898728
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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