A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562140



Internal ID20935211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:72109273..72109397hg38UCSC Ensembl
chr5:71405100..71405224hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267045
Samples
Known GenesMAP1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562140
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