A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3199158



Internal ID22348784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:177011077..177012580hg38UCSC Ensembl
chr5:176438078..176439581hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg381504
hg191504
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14325350
SamplesHG00512
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3199158
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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