A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7576n152



Internal ID22823279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:154583464..154583543hg38UCSC Ensembl
chr5:153963024..153963103hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3286899, nsv3205234, nsv3525552
SamplesHG00512, NA19240, HG00514
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)dgv7576n152
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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