A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5839703



Internal ID22614638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:59170135..59226509hg38UCSC Ensembl
chr4:60035853..60092227hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3856375
hg1956375
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17496386, nssv17496385
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5839703
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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