A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5922432



Internal ID22697657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66552416..66562726hg38UCSC Ensembl
chr11:66319887..66330197hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3810311
hg1910311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17357425
Samples
Known GenesACTN3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5922432
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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