A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539587



Internal ID20912883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:224229373..224229969hg38UCSC Ensembl
chr1:224417075..224417671hg19UCSC Ensembl
Cytoband1q42.11
Allele length
AssemblyAllele length
hg38597
hg19597
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249358
Samples
Known GenesNVL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539587
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer