A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18193763



Internal ID20760803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:85893602..85904715hg38UCSC Ensembl
chr9:88508517..88519630hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3811114
hg1911114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6440082
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18193763
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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