A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6143172



Internal ID342373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:96039908..96040735hg38UCSC Ensembl
chr11:95773072..95773899hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38828
hg19828
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17049292
Samples
Known GenesMAML2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6143172
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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