A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596697



Internal ID20969768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:21109454..21737143hg38UCSC Ensembl
chr21:22481772..23109463hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38627690
hg19627692
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254225
Samples
Known GenesLINC00317, NCAM2, RNU6-67P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596697
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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