A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18195682



Internal ID20762722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97930780..97942771hg38UCSC Ensembl
chr9:100693062..100705053hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3811992
hg1911992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6439016
Supporting Variants
Samples
Known GenesHEMGN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18195682
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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