A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5838193



Internal ID22613128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:182879816..182884800hg38UCSC Ensembl
chr4:183800969..183805953hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg384985
hg194985
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17491315
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5838193
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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