A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18222826



Internal ID20789866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:52803668..52845943hg38UCSC Ensembl
chr6:52668466..52710741hg19UCSC Ensembl
Cytoband6p12.2
Allele length
AssemblyAllele length
hg3842276
hg1942276
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6408785
Supporting Variants
Samples
Known GenesGSTA1, GSTA5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18222826
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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