A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6599127



Internal ID20972198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:31479783..31480494hg38UCSC Ensembl
chr20:30067586..30068297hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38712
hg19712
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251713
Samples
Known GenesREM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6599127
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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