A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18135153



Internal ID20702193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:77885698..77886925hg38UCSC Ensembl
chr5:77181522..77182749hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg381228
hg191228
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6412379
Supporting Variants
Samples
Known GenesLOC101929154
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18135153
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00095


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