A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540377



Internal ID20913668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:10118902..10120373hg38UCSC Ensembl
chr1:10178960..10180431hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg381472
hg191472
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249207
Samples
Known GenesUBE4B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540377
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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