A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6024820



Internal ID21934163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66552416..66562733hg38UCSC Ensembl
chr11:66319887..66330204hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3810318
hg1910318
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17579447
Samples
Known GenesACTN3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6024820
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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