A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8262n152



Internal ID22823965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:169765854..169766002hg38UCSC Ensembl
chr6:170165950..170166098hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38149
hg19149
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3528623, nsv3285946
SamplesNA19239, HG00732, NA19240
Known GenesERMARD
MethodMerging
Sequencing
AnalysisMultiple analysis algorthms
PhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformIllumina HiSeq
See merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv8262n152
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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