A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18171632



Internal ID20738672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:101422537..101469860hg38UCSC Ensembl
chr9:104184819..104232142hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3847324
hg1947324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6447947
Supporting Variants
Samples
Known GenesALDOB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18171632
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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