A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18064657



Internal ID20631697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:79965701..79967800hg38UCSC Ensembl
chr1:80431386..80433485hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6328543
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18064657
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00026


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