A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17046576



Internal ID98861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61684654..61685037hg38UCSC Ensembl
chr11:61452126..61452509hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38384
hg19384
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5560153
Supporting Variants
Samples
Known GenesDAGLA
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17046576
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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