A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18201694



Internal ID20768735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:178945674..178957726hg38UCSC Ensembl
chr1:178914809..178926861hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg3812053
hg1912053
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6328677
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18201694
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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