A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5830956



Internal ID22605891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:128088109..128103032hg38UCSC Ensembl
chr2:128845683..128860606hg19UCSC Ensembl
Cytoband2q14.3
Allele length
AssemblyAllele length
hg3814924
hg1914924
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17486300
Samples
Known GenesUGGT1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5830956
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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