A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5829082



Internal ID22604017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:202332503..202336063hg38UCSC Ensembl
chr1:202301631..202305191hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg383561
hg193561
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17468154, nssv17463273
Samples
Known GenesUBE2T
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5829082
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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