A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5890605



Internal ID22665633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:133935961..133936581hg38UCSC Ensembl
chr5:133271652..133272272hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg38621
hg19621
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17419339
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5890605
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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