A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17049897



Internal ID101160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:87558581..87558626hg38UCSC Ensembl
chr11:87269473..87269518hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3846
hg1946
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5558612
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17049897
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00843


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