A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3529207



Internal ID22398600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:111697177..111697285hg38UCSC Ensembl
chr13:112349524..112349632hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14369444, nssv14369445
SamplesHG00732, HG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3529207
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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