A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18187766



Internal ID20754806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:24123694..24161656hg38UCSC Ensembl
chr9:24123692..24161654hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3837963
hg1937963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6426899
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18187766
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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