A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv93n152



Internal ID22815796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:7864877..7865284hg38UCSC Ensembl
chr1:7924937..7925344hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg38408
hg19408
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3282471, nsv3280685
SamplesNA19240, HG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv93n152
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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