A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6022007



Internal ID21931350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66538095..66551804hg38UCSC Ensembl
chr11:66305566..66319275hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3813710
hg1913710
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17595362
Samples
Known GenesACTN3, ZDHHC24
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6022007
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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