A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544187



Internal ID20917426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:36017772..36018128hg38UCSC Ensembl
chr1:36483373..36483729hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38357
hg19357
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251034
Samples
Known GenesAGO3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544187
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