A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6599389



Internal ID20972460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34371156..34371290hg38UCSC Ensembl
chr20:32958962..32959096hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251817
Samples
Known GenesITCH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6599389
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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