A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5832682



Internal ID22607617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:4620845..4622251hg38UCSC Ensembl
chr2:4668435..4669841hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg381407
hg191407
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17486128, nssv17486129
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5832682
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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