A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326686



Internal ID20859823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:47020004..47190521hg38UCSC Ensembl
chr1:47485676..47656193hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg38170518
hg19170518
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061590
Samples
Known GenesCYP4A22, CYP4X1, CYP4Z1, LINC00853, PDZK1IP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326686
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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