A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3190444



Internal ID22341305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:101910376..101910523hg38UCSC Ensembl
chr8:102922604..102922751hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38148
hg19148
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9277n152
Supporting Variantsnssv14402148
SamplesNA19240
Known GenesNCALD
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3190444
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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