A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18215636



Internal ID20782676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:203826..494738hg38UCSC Ensembl
chr5:203941..494853hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38290913
hg19290913
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6387377
Supporting Variants
Samples
Known GenesAHRR, C5orf55, CCDC127, EXOC3, LOC102467073, PDCD6, PP7080, SDHA, SLC9A3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18215636
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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