A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17993715



Internal ID20560755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:58338064..58338547hg38UCSC Ensembl
chr11:58105537..58106020hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38484
hg19484
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6464086
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17993715
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00102


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