A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17051771



Internal ID102360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134133994..134137736hg38UCSC Ensembl
chr11:134003889..134007631hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg383743
hg193743
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5494024
Supporting Variants
Samples
Known GenesJAM3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17051771
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000624


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