A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5831394



Internal ID22606329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:160284561..160290550hg38UCSC Ensembl
chr2:161141072..161147061hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg385990
hg195990
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17480593, nssv17480592
Samples
Known GenesRBMS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5831394
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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