A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18132654



Internal ID20699694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:68109111..68110265hg38UCSC Ensembl
chr5:67404939..67406093hg19UCSC Ensembl
Cytoband5q13.1
Allele length
AssemblyAllele length
hg381155
hg191155
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6401355
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18132654
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00233


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