A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18125387



Internal ID20692427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:139135914..139139753hg38UCSC Ensembl
chr5:138471603..138475442hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg383840
hg193840
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6396510
Supporting Variants
Samples
Known GenesSIL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18125387
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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