A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5834157



Internal ID22609092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:9737802..9763402hg38UCSC Ensembl
chr2:9877931..9903531hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3825601
hg1925601
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17483051
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5834157
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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