A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223913



Internal ID20790953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:52810953..52886773hg38UCSC Ensembl
chr6:52675751..52751571hg19UCSC Ensembl
Cytoband6p12.2
Allele length
AssemblyAllele length
hg3875821
hg1975821
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6396242
Supporting Variants
Samples
Known GenesGSTA5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223913
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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