A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3198787



Internal ID22348470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:81334367..81334465hg38UCSC Ensembl
chr8:82246602..82246700hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14438511, nssv14373178
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)nsv3198787
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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