A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5837776



Internal ID22612711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:158474953..158477580hg38UCSC Ensembl
chr4:159396105..159398732hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg382628
hg192628
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1607n209
Supporting Variantsnssv17499742
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5837776
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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