A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566571



Internal ID20939642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:31516082..31517090hg38UCSC Ensembl
chr4:31517704..31518712hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg381009
hg191009
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18265706
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566571
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