A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14382432



Internal ID22267674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78993266..78993266hg38UCSC Ensembl
chr15:79285608..79285608hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38632
hg19632
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3561057
Supporting Variants
SamplesNA19238
Known GenesRASGRF1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14382432
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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