A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538631



Internal ID20911944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:157093509..157094912hg38UCSC Ensembl
chr1:157063301..157064704hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg381404
hg191404
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv394n223
Supporting Variantsnssv18247757
Samples
Known GenesETV3L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538631
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