A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18126792



Internal ID20693832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:153891757..153917801hg38UCSC Ensembl
chr5:153271317..153297361hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg3826045
hg1926045
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6405423
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18126792
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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