A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17608066



Internal ID21800113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134138399..134138472hg38UCSC Ensembl
chr11:134008294..134008367hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6035781
Supporting Variants
Samples
Known GenesJAM3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17608066
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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