A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3209038



Internal ID22357175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:49083235..49161472hg38UCSC Ensembl
chr4:49085252..49163489hg19UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg3878238
hg1978238
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6583n152
Supporting Variantsnssv14409205
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)nsv3209038
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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