A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17047642



Internal ID99636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:68686213..68687167hg38UCSC Ensembl
chr11:68453681..68454635hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg38955
hg19955
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5554536
Supporting Variants
Samples
Known GenesGAL
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17047642
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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