A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3201631



Internal ID22350902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:169898101..169902950hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg384850
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8265n152
Supporting Variantsnssv14437531, nssv14387065
SamplesNA19240, HG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3201631
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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