A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189573



Internal ID20756613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:82393341..82404255hg38UCSC Ensembl
chr9:85008256..85019170hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3810915
hg1910915
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6449330
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189573
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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