A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3525199



Internal ID22394575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:90706472..90706753hg38UCSC Ensembl
chr5:90002289..90002570hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38282
hg19282
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14322034
SamplesNA19239
Known GenesGPR98
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3525199
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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