A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17592972



Internal ID21785015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:8217875..8217937hg38UCSC Ensembl
chr11:8239422..8239484hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6032681
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17592972
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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