A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1607n209



Internal ID22827682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:158474953..158478180hg38UCSC Ensembl
chr4:159396105..159399332hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg383228
hg193228
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5837776, nsv5837777
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv1607n209
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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