A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191935



Internal ID20758975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:73518201..73520300hg38UCSC Ensembl
chr9:76133117..76135216hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6452185
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191935
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00055


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