A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18065051



Internal ID20632091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:84360430..84360998hg38UCSC Ensembl
chr1:84826113..84826681hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38569
hg19569
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6331198
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18065051
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0005


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