A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17993545



Internal ID20560585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:68125886..68133241hg38UCSC Ensembl
chr11:67893353..67900708hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg387356
hg197356
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6475138
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17993545
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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