A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17493711



Internal ID22551640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:116254377..116290701hg38UCSC Ensembl
chr5:115590074..115626398hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3836325
hg1936325
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5841228
Supporting Variants
Samples
Known GenesCOMMD10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17493711
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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