A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5836930



Internal ID22611865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:99027694..99084221hg38UCSC Ensembl
chr3:98746538..98803065hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg3856528
hg1956528
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17497534
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5836930
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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