A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17044962



Internal ID97722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:43654591..43678617hg38UCSC Ensembl
chr11:43676141..43700167hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3824027
hg1924027
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5496021
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17044962
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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