A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6334029



Internal ID20867210
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 StatusM
Merged Variants
Supporting Variantsnssv18203540
Samples
Known GenesPHACTR4, RCC1, SNHG3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6334029
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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