A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3193538



Internal ID22343973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:33744673..33745069hg38UCSC Ensembl
chr3:33786165..33786561hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38397
hg19397
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14307367, nssv14307366, nssv14307368
SamplesHG00512, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3193538
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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