A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6542760



Internal ID20916012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:229360990..229361462hg38UCSC Ensembl
chr1:229496737..229497209hg19UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg38473
hg19473
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250320
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6542760
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