A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5829187



Internal ID22604122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:212172783..212175783hg38UCSC Ensembl
chr1:212346125..212349125hg19UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg383001
hg193001
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17453118
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5829187
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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