A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6394n152



Internal ID22822097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:2334737..2334826hg38UCSC Ensembl
chr4:2336464..2336553hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3282447, nsv3203114, nsv3282752
SamplesNA19238, NA19240, HG00514
Known GenesZFYVE28
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)dgv6394n152
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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