A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5839281



Internal ID22614216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:38435578..38445434hg38UCSC Ensembl
chr4:38437199..38447055hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg389857
hg199857
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17494487
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5839281
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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