A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5888620



Internal ID22663628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:108822843..108822923hg38UCSC Ensembl
chr5:108158544..108158624hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17427777
Samples
Known GenesFER
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5888620
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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