A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18194043



Internal ID20761083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:33836106..33886375hg38UCSC Ensembl
chr9:33836104..33886373hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3850270
hg1950270
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6437134
Supporting Variants
Samples
Known GenesUBE2R2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18194043
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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