A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6545396



Internal ID20918627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9953854..9955334hg38UCSC Ensembl
chr1:10013912..10015392hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg381481
hg191481
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18252817
Samples
Known GenesNMNAT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6545396
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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