A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17600862



Internal ID21792909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134133993..134138138hg38UCSC Ensembl
chr11:134003888..134008033hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg384146
hg194146
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6022942
Supporting Variants
Samples
Known GenesJAM3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17600862
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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