A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6599057



Internal ID20972128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:9783914..9785576hg38UCSC Ensembl
chr4_gl000193_random:51228..52890hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg381663
hg191663
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254262
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6599057
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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