A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17991736



Internal ID20558776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:45767690..45770069hg38UCSC Ensembl
chr11:45789241..45791620hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg382380
hg192380
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6472910
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17991736
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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