A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3211630



Internal ID22359123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:73045917..73046584hg38UCSC Ensembl
chr13:73620055..73620722hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg38668
hg19668
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14366086, nssv14366087, nssv14366085
SamplesNA19238, HG00731, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3211630
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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