A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554616



Internal ID20927710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9954930..9956272hg38UCSC Ensembl
chr1:10014988..10016330hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg381343
hg191343
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18252818
Samples
Known GenesNMNAT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554616
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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