A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18175081



Internal ID20742121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:114806946..114807738hg38UCSC Ensembl
chr9:117569226..117570018hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38793
hg19793
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6438793
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18175081
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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