A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549969



Internal ID20923120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:110286146..110287353hg38UCSC Ensembl
chr1:110828768..110829975hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg381208
hg191208
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247370
Samples
Known GenesLOC440600
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549969
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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