A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3525404



Internal ID22394782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:41526558..41527299hg38UCSC Ensembl
chr1:41992229..41992970hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38742
hg19742
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14363323, nssv14363324, nssv14363322, nssv14363321, nssv14363325, nssv14363326
SamplesNA19238, NA19239, HG00731, HG00732, NA19240, HG00733
Known GenesHIVEP3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3525404
Frequency
Sample Size9
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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