A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8775n152



Internal ID22824478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139424842..139425207hg38UCSC Ensembl
chr7:139109588..139109953hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38366
hg19366
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3528430, nsv3288565
SamplesNA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513
Known GenesLOC100129148
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)dgv8775n152
Frequency
Sample Size9
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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