A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316606



Internal ID20849686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:240400601..240403100hg38UCSC Ensembl
chr1:240563901..240566400hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg382500
hg192500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202538
Samples
Known GenesFMN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316606
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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