A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18059232



Internal ID20626272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:228889843..228890390hg38UCSC Ensembl
chr1:229025590..229026137hg19UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg38548
hg19548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6320388
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18059232
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00014


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