A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6994n152



Internal ID22822697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:182830858..182835584hg38UCSC Ensembl
chr4:183752011..183756737hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg384727
hg194727
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3184462, nsv3185529
SamplesHG00733, 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)dgv6994n152
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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