A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3561237



Internal ID22430018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:6814671..6814671hg38UCSC Ensembl
chr19:6814682..6814682hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14291445, nssv14291444
SamplesNA19239, NA19240
Known GenesVAV1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3561237
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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