A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18205178



Internal ID20772218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:86506956..86549222hg38UCSC Ensembl
chr1:86972639..87014905hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg3842267
hg1942267
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6318508
Supporting Variants
Samples
Known GenesCLCA4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18205178
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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