A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18200404



Internal ID20767444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150847761..150870903hg38UCSC Ensembl
chr1:150820237..150843379hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3823143
hg1923143
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6333911
Supporting Variants
Samples
Known GenesARNT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18200404
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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