A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5833893



Internal ID22608828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:100203810..100206059hg38UCSC Ensembl
chr3:99922654..99924903hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg382250
hg192250
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17483095
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5833893
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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