A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7957n152



Internal ID22823660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:69749840..69750083hg38UCSC Ensembl
chr6:70459732..70459975hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38244
hg19244
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3286733, nsv3529567
SamplesNA19238, NA19239, NA19240
Known GenesLMBRD1
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)dgv7957n152
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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