A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3202868



Internal ID22351969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:180285961..180286303hg38UCSC Ensembl
chr5:179712961..179713303hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38343
hg19343
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14323462
SamplesHG00514
Known GenesMAPK9
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3202868
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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