A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5838316



Internal ID22613251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:156671682..156683899hg38UCSC Ensembl
chr4:157592834..157605051hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3812218
hg1912218
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17499732, nssv17493540
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5838316
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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