A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203540



Internal ID20770580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28488316..28514582hg38UCSC Ensembl
chr1:28814828..28841094hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg3826267
hg1926267
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6334029
Supporting Variants
Samples
Known GenesPHACTR4, RCC1, SNHG3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203540
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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