A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5830871



Internal ID22605806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:101314319..101323355hg38UCSC Ensembl
chr2:101930781..101939817hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg389037
hg199037
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17484883
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5830871
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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