A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6599837



Internal ID20972908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:19130361..23504700hg38UCSC Ensembl
chr21:20502679..24877019hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg384374340
hg194374341
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4557n223
Supporting Variantsnssv18254195
Samples
Known GenesD21S2088E, LINC00308, LINC00317, LINC00320, NCAM2, RNU6-67P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6599837
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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