A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576718



Internal ID20949789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:5851686..5852882hg38UCSC Ensembl
chr10:5893649..5894845hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg381197
hg191197
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv605n223
Supporting Variantsnssv18218765
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576718
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