A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556821



Internal ID20929892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:128731823..128732247hg38UCSC Ensembl
chr3:128450666..128451090hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg38425
hg19425
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259601
Samples
Known GenesRAB7A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556821
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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