A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18186952



Internal ID20753992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93374201..93377800hg38UCSC Ensembl
chr9:96136483..96140082hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg383600
hg193600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6441220
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18186952
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00049


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