A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17051309



Internal ID102066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:101251729..101252554hg38UCSC Ensembl
chr11:101122460..101123285hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38826
hg19826
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5554188
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17051309
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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