A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3210160



Internal ID22358122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:89097202..89097290hg38UCSC Ensembl
chr4:90018353..90018441hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6734n152
Supporting Variantsnssv14434765
SamplesHG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3210160
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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