A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14359625



Internal ID22270318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60525910..60525910hg38UCSC Ensembl
chr11:60293383..60293383hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3559690
Supporting Variants
SamplesNA19239
Known GenesMS4A13
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14359625
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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