A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18252819



Internal ID20819859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9955427..9956678hg38UCSC Ensembl
chr1:10015485..10016736hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg381252
hg191252
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6542107
Supporting Variants
Samples
Known GenesNMNAT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18252819
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00012


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