A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5833950



Internal ID22608885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:117086398..117092159hg38UCSC Ensembl
chr3:116805245..116811006hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg385762
hg195762
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17483816
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5833950
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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