A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562791



Internal ID20935862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:80630036..80630608hg38UCSC Ensembl
chr5:79925855..79926427hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg38573
hg19573
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268989
Samples
Known GenesDHFR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562791
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