A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596460



Internal ID20969531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:25581613..25582548hg38UCSC Ensembl
chr20:25562249..25563184hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg38936
hg19936
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4426n223
Supporting Variantsnssv18254317
Samples
Known GenesNINL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596460
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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