A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14358587



Internal ID22142970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:77005954..77005954hg38UCSC Ensembl
chr11:76716998..76716998hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3559704
Supporting Variants
SamplesHG00513
Known GenesACER3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14358587
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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