A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18127142



Internal ID20694182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:132794097..132813781hg38UCSC Ensembl
chr5:132129789..132149473hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3819685
hg1919685
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6410729
Supporting Variants
Samples
Known GenesSOWAHA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18127142
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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