A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17042809



Internal ID96243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:8729180..8729234hg38UCSC Ensembl
chr11:8750727..8750781hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5513175
Supporting Variants
Samples
Known GenesST5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17042809
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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