A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5829117



Internal ID22604052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:193087616..193089046hg38UCSC Ensembl
chr1:193056746..193058176hg19UCSC Ensembl
Cytoband1q31.2
Allele length
AssemblyAllele length
hg381431
hg191431
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17467136, nssv17456759
Samples
Known GenesTROVE2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5829117
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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