A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18186856



Internal ID20753896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:36295876..36300408hg38UCSC Ensembl
chr9:36295873..36300405hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg384533
hg194533
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6451106
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18186856
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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