A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17995747



Internal ID20562787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:97121393..97233147hg38UCSC Ensembl
chr11:96992393..97104147hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38111755
hg19111755
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6458395
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17995747
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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