A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574774



Internal ID20947845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:95571003..95572782hg38UCSC Ensembl
chr5:94906707..94908486hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg381780
hg191780
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267739
Samples
Known GenesARSK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6574774
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