A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6321559



Internal ID20854666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:46907517..47090164hg38UCSC Ensembl
chr1:47373189..47555836hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg38182648
hg19182648
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201388
Samples
Known GenesCYP4A11, CYP4X1, CYP4Z1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6321559
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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