A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16287331



Internal ID20496549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66552416..66562720hg38UCSC Ensembl
chr11:66319887..66330191hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3810305
hg1910305
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4738491
Supporting Variants
Samples
Known GenesACTN3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16287331
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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