A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557455



Internal ID20930526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:146250270..146250979hg38UCSC Ensembl
chr5:145629833..145630542hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38710
hg19710
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268027
Samples
Known GenesRBM27
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557455
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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