A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6599782



Internal ID20972853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:25581000..25581486hg38UCSC Ensembl
chr21:26953312..26953798hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg38487
hg19487
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18252949
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6599782
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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