A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6718n152



Internal ID22822421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:86021302..86021463hg38UCSC Ensembl
chr4:86942455..86942616hg19UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg38162
hg19162
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3240867, nsv3240508
SamplesNA19240, HG00514
Known GenesMAPK10
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv6718n152
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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