A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14328584



Internal ID22206613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:69122018..69122018hg38UCSC Ensembl
chr6:69831910..69831910hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3564605
Supporting Variants
SamplesHG00732
Known GenesBAI3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14328584
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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