A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18064249



Internal ID20631289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:79191507..79298740hg38UCSC Ensembl
chr1:79657192..79764425hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38107234
hg19107234
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6318959
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18064249
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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