A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7650n152



Internal ID22823353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:177673403..177682164hg38UCSC Ensembl
chr5:177100404..177109165hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg388762
hg198762
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3192679, nsv3192100
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)dgv7650n152
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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