A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17992883



Internal ID20559923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:71596586..71623209hg38UCSC Ensembl
chr11:71307632..71334255hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3826624
hg1926624
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6473660
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17992883
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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