A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3223636



Internal ID22367340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:88347709..88347863hg38UCSC Ensembl
chr13:88999964..89000118hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2367n152
Supporting Variantsnssv14402349
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3223636
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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