A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578485



Internal ID20951556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28570981..28572331hg38UCSC Ensembl
chr10:28859910..28861260hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg381351
hg191351
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234058
Samples
Known GenesWAC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578485
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