A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17990597



Internal ID20557638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:31987401..31987800hg38UCSC Ensembl
chr11:32008947..32009346hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38400
hg19400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6438393
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17990597
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.07585


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