A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573221



Internal ID20946292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:119325162..119334862hg38UCSC Ensembl
chr5:118660857..118670557hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg389701
hg199701
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18266175
Samples
Known GenesTNFAIP8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573221
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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