A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556655



Internal ID20929726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:43051646..43052089hg38UCSC Ensembl
chr5:43051748..43052191hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg38444
hg19444
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268383
Samples
Known GenesLOC648987
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556655
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