A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7975n152



Internal ID22823678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:74543279..74543340hg38UCSC Ensembl
chr6:75252995..75253056hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3285383, nsv3191205
SamplesNA19239, 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)dgv7975n152
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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