A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326244



Internal ID20859378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:84483347..84484766hg38UCSC Ensembl
chr1:84949030..84950449hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg381420
hg191420
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205157
Samples
Known GenesRPF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326244
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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