A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190266



Internal ID20757306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:24972735..25087811hg38UCSC Ensembl
chr9:24972733..25087809hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38115077
hg19115077
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6418768
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190266
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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