A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7751n152



Internal ID22823454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:14008771..14008853hg38UCSC Ensembl
chr6:14009002..14009084hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3198549, nsv3203359
SamplesHG00731, HG00733
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)dgv7751n152
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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