A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18132796



Internal ID20699836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:44570922..44577727hg38UCSC Ensembl
chr5:44571024..44577829hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg386806
hg196806
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6391891
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18132796
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00235


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