A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6319710



Internal ID20852805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:47041379..47060032hg38UCSC Ensembl
chr1:47507051..47525704hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg3818654
hg1918654
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201391
Samples
Known GenesCYP4X1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6319710
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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