A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18050282



Internal ID20617322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:104161780..104177409hg38UCSC Ensembl
chr1:104704402..104720031hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3815630
hg1915630
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6321586
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18050282
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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