A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17994147



Internal ID20561187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:77549229..77549668hg38UCSC Ensembl
chr11:77260274..77260713hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38440
hg19440
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6457707
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17994147
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00091


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