A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5829206



Internal ID22604141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:221860115..221861170hg38UCSC Ensembl
chr1:222033457..222034512hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg381056
hg191056
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17463600, nssv17464402
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5829206
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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