A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5831256



Internal ID22606191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:128113237..128123619hg38UCSC Ensembl
chr2:128870811..128881193hg19UCSC Ensembl
Cytoband2q14.3
Allele length
AssemblyAllele length
hg3810383
hg1910383
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17486302
Samples
Known GenesUGGT1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5831256
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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