A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581398



Internal ID20954469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:50706344..50706900hg38UCSC Ensembl
chr17:48783705..48784261hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg38557
hg19557
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18245166
Samples
Known GenesANKRD40
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581398
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