A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3561057



Internal ID22429850
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14381177, nssv14382432, nssv14390147
SamplesNA19238, NA19239, HG00731
Known GenesRASGRF1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3561057
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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