A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598338



Internal ID20971409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:32671915..32672502hg38UCSC Ensembl
chr21:34044225..34044812hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg38588
hg19588
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254025
Samples
Known GenesSYNJ1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598338
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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