A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5830878



Internal ID22605813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:105221533..105224167hg38UCSC Ensembl
chr2:105837990..105840624hg19UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg382635
hg192635
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17484909
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5830878
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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