A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6430n152



Internal ID22822133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:6725783..6725853hg38UCSC Ensembl
chr4:6727510..6727580hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3193457, nsv3195741
SamplesNA19238, NA19240
Known Genes
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)dgv6430n152
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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