A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3225131



Internal ID22368354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:64278106..64278190hg38UCSC Ensembl
chr20:62909459..62909543hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14300582, nssv14300581, nssv14300580
SamplesHG00731, HG00732, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3225131
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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