A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5833454



Internal ID22608389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:7872723..7878510hg38UCSC Ensembl
chr2:8012854..8018641hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg385788
hg195788
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17488102, nssv17481645
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5833454
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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