A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6963n152



Internal ID22822666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:174320510..174323153hg38UCSC Ensembl
chr4:175241661..175244304hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg382644
hg192644
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3181346, nsv3176548, nsv3177969
SamplesNA19240, HG00733, HG00514
Known GenesCEP44
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv6963n152
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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