A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18213129



Internal ID20780169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:122068446..122176041hg38UCSC Ensembl
chr5:121404141..121511736hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg38107596
hg19107596
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6403661
Supporting Variants
Samples
Known GenesLOC100505841, LOX, ZNF474
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18213129
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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