A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18052437



Internal ID20619477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:160018437..160018863hg38UCSC Ensembl
chr1:159988227..159988653hg19UCSC Ensembl
Cytoband1q23.2
Allele length
AssemblyAllele length
hg38427
hg19427
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6318791
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18052437
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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