A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5829840



Internal ID22604775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32600437..32601536hg38UCSC Ensembl
chr1:33066038..33067137hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17466619, nssv17457220
Samples
Known GenesZBTB8A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5829840
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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