A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17047297



Internal ID99375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:45758434..45785223hg38UCSC Ensembl
chr11:45779985..45806774hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3826790
hg1926790
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6143810
Supporting Variants
Samples
Known GenesDKFZp779M0652
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17047297
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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