A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572990



Internal ID20946061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:58837613..58838394hg38UCSC Ensembl
chr5:58133440..58134221hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38782
hg19782
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268918
Samples
Known GenesRAB3C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572990
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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