A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17041450



Internal ID95339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:15113728..15113817hg38UCSC Ensembl
chr11:15135274..15135363hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5506061
Supporting Variants
Samples
Known GenesINSC
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17041450
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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