A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3564159



Internal ID22432893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:180797843..180797843hg38UCSC Ensembl
chr5:180224843..180224843hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14324109
SamplesHG00731
Known GenesMGAT1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3564159
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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