A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5832620



Internal ID22607555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:3312603..3319522hg38UCSC Ensembl
chr2:3316374..3323293hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg386920
hg196920
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17484160
Samples
Known GenesTSSC1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5832620
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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