A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571060



Internal ID20944131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38777500..38778101hg38UCSC Ensembl
chr8:38635018..38635619hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38602
hg19602
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277944
Samples
Known GenesTACC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571060
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