A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14340414



Internal ID22265085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:30786497..30786497hg38UCSC Ensembl
chr8:30644013..30644013hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3565461
Supporting Variants
SamplesNA19238
Known GenesPPP2CB
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14340414
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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