A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547739



Internal ID20920940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:46939751..47139205hg38UCSC Ensembl
chr1:47405423..47604877hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg38199455
hg19199455
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251145
Samples
Known GenesCYP4A11, CYP4A22, CYP4X1, CYP4Z1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547739
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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