A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581977



Internal ID20955048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68966020..68966429hg38UCSC Ensembl
chr10:70725776..70726185hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38410
hg19410
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225423
Samples
Known GenesDDX21
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581977
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