A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18129701



Internal ID20696741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:34057169..34066958hg38UCSC Ensembl
chr5:34057274..34067063hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg389790
hg199790
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6394488
Supporting Variants
Samples
Known GenesC1QTNF3-AMACR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18129701
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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