A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5831846



Internal ID22606781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:201135967..201139854hg38UCSC Ensembl
chr2:202000690..202004577hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg383888
hg193888
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17489262
Samples
Known GenesCFLAR
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5831846
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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