A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5901593



Internal ID22676744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:159208004..159262540hg38UCSC Ensembl
chr5:158635012..158689548hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg3854537
hg1954537
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17410570
Samples
Known GenesRNF145
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5901593
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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