A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231878



Internal ID20798918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:132070587..132070911hg38UCSC Ensembl
chr8:133082834..133083158hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6416205
Supporting Variants
Samples
Known GenesHHLA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231878
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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