A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18060284



Internal ID20627324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25126566..25132117hg38UCSC Ensembl
chr1:25453057..25458608hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg385552
hg195552
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6331273
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18060284
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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