A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5906471



Internal ID22681672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:123236803..123251646hg38UCSC Ensembl
chr5:122572497..122587340hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg3814844
hg1914844
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17418488
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5906471
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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