A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17993659



Internal ID20560699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:57881057..57890493hg38UCSC Ensembl
chr11:57648529..57657965hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg389437
hg199437
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6459353
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17993659
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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