A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566766



Internal ID20939837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:149348999..149350046hg38UCSC Ensembl
chr5:148728562..148729609hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg381048
hg191048
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268668
Samples
Known GenesGRPEL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566766
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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