A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544721



Internal ID20917958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:63633019..63633766hg38UCSC Ensembl
chr1:64098690..64099437hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38748
hg19748
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv215n223
Supporting Variantsnssv18250606
Samples
Known GenesPGM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544721
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