A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571352



Internal ID20944423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:146242590..146243185hg38UCSC Ensembl
chr5:145622153..145622748hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38596
hg19596
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268026
Samples
Known GenesRBM27
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571352
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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