A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18180221



Internal ID20747261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:74997860..74998385hg38UCSC Ensembl
chr9:77612776..77613301hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38526
hg19526
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6440876
Supporting Variants
Samples
Known GenesC9orf41
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18180221
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00051


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