A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203606



Internal ID20770646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32556315..32603375hg38UCSC Ensembl
chr1:33021916..33068976hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg3847061
hg1947061
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6333415
Supporting Variants
Samples
Known GenesZBTB8A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203606
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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