A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17046556



Internal ID98847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61399835..61401212hg38UCSC Ensembl
chr11:61167307..61168684hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg381378
hg191378
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5511344
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17046556
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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