A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6097337



Internal ID22006570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61817841..61817841hg38UCSC Ensembl
chr11:61585313..61585313hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38141
hg19141
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17593392
Samples
Known GenesFADS2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6097337
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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