A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14357631



Internal ID22182522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33880285..33880285hg38UCSC Ensembl
chr11:33901831..33901831hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3559457
Supporting Variants
SamplesHG00514
Known GenesLMO2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14357631
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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