A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv81n152



Internal ID22815784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:5667636..5667833hg38UCSC Ensembl
chr1:5727696..5727893hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg38198
hg19198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3282354, nsv3192323
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)dgv81n152
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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