A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18235017



Internal ID20802057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:131881559..131962780hg38UCSC Ensembl
chr8:132893806..132975027hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3881222
hg1981222
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6429198
Supporting Variants
Samples
Known GenesEFR3A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18235017
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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