A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18213896



Internal ID20780936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:152297007..152401131hg38UCSC Ensembl
chr5:151676568..151780692hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg38104125
hg19104125
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6401562
Supporting Variants
Samples
Known GenesNMUR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18213896
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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