A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17606304



Internal ID21798351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:112287655..112287789hg38UCSC Ensembl
chr11:112158378..112158512hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6040244
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17606304
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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