A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17587061



Internal ID21779104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:31174445..31174948hg38UCSC Ensembl
chr11:31195992..31196495hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38504
hg19504
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6028371
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17587061
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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