A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6599587



Internal ID20972658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:49041960..49042330hg38UCSC Ensembl
chr20:47658497..47658867hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38371
hg19371
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18252225
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6599587
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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