A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18195092



Internal ID20762132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:26452714..26670586hg38UCSC Ensembl
chr9:26452712..26670584hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg38217873
hg19217873
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6423749
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18195092
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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