A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3563234



Internal ID22431974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:15737522..15737522hg38UCSC Ensembl
chr3:15779029..15779029hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14305422, nssv14305423, nssv14305428, nssv14305421, nssv14305424, nssv14305425, nssv14305427, nssv14305426
SamplesHG00512, NA19238, NA19239, HG00731, NA19240, HG00733, HG00513, HG00514
Known GenesANKRD28
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3563234
Frequency
Sample Size9
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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