A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3225192



Internal ID22368397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:30390583..30391089hg38UCSC Ensembl
chr13:30964720..30965226hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg38507
hg19507
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14367964
SamplesHG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3225192
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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