A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596594



Internal ID20969665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:38709562..38710926hg38UCSC Ensembl
chr21:40081486..40082850hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg381365
hg191365
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254741
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596594
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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