A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18268937



Internal ID20835977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:60558085..60879487hg38UCSC Ensembl
chr5:59853912..60175314hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg38321403
hg19321403
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6573220
Supporting Variants
Samples
Known GenesDEPDC1B, ELOVL7, ERCC8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18268937
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00013


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