A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18132906



Internal ID20699946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:81552684..81592722hg38UCSC Ensembl
chr5:80848503..80888541hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg3840039
hg1940039
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6395677
Supporting Variants
Samples
Known GenesSSBP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18132906
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00041


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