A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5839988



Internal ID22614923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:60413670..60463563hg38UCSC Ensembl
chr4:61279388..61329281hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3849894
hg1949894
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17496429
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5839988
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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