A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17044871



Internal ID97660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:23419129..23419189hg38UCSC Ensembl
chr11:23440675..23440735hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5512621
Supporting Variants
Samples
Known GenesMIR8054
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17044871
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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