A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17049732



Internal ID101049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:86985926..86995824hg38UCSC Ensembl
chr11:86696968..86706866hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg389899
hg199899
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5509721
Supporting Variants
Samples
Known GenesLOC100506368
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17049732
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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