A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5837651



Internal ID22612586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:124473760..124478690hg38UCSC Ensembl
chr4:125394915..125399845hg19UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg384931
hg194931
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17490172
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5837651
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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