A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5839057



Internal ID22613992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:48971181..48990376hg38UCSC Ensembl
chr4:48973198..48992393hg19UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg3819196
hg1919196
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17495281, nssv17495280
Samples
Known GenesCWH43
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5839057
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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