A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17597328



Internal ID21789371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:87815584..87815718hg38UCSC Ensembl
chr11:87526476..87526610hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6025143
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17597328
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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