A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18214982



Internal ID20782022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:88320601..88361500hg38UCSC Ensembl
chr5:87616418..87657317hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3840900
hg1940900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6395800
Supporting Variants
Samples
Known GenesTMEM161B-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18214982
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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