A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1004n152



Internal ID22816707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86469244..86469310hg38UCSC Ensembl
chr10:88229001..88229067hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3198316, nsv3206081, nsv3204045
SamplesNA19240, HG00733, HG00514
Known GenesWAPAL
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv1004n152
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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