A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18054936



Internal ID20621976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:189028326..189888533hg38UCSC Ensembl
chr1:188997457..189857663hg19UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg38860208
hg19860207
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6324498
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18054936
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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