A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6985n152



Internal ID22822688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:180567348..180567403hg38UCSC Ensembl
chr4:181488501..181488556hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3192881, nsv3209597
SamplesHG00731, 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)dgv6985n152
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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