A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231269



Internal ID20798309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:52849393..52994904hg38UCSC Ensembl
chr6:52714191..52859702hg19UCSC Ensembl
Cytoband6p12.2
Allele length
AssemblyAllele length
hg38145512
hg19145512
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6396059
Supporting Variants
Samples
Known GenesGSTA3, GSTA4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231269
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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