A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17992705



Internal ID20559745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:69470901..69471500hg38UCSC Ensembl
chr11:69285669..69286268hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg38600
hg19600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6463532
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17992705
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.07047


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