A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14326815



Internal ID22206454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:25335938..25335938hg38UCSC Ensembl
chr6:25336166..25336166hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3564351
Supporting Variants
SamplesHG00732
Known GenesLRRC16A
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14326815
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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