A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv757n152



Internal ID22816460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4031226..4031302hg38UCSC Ensembl
chr10:4073418..4073494hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3528722, nsv3221022
SamplesHG00731, HG00732, HG00733
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)dgv757n152
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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