A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538382



Internal ID20911699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:135210356..135211026hg38UCSC Ensembl
chr2:135967926..135968596hg19UCSC Ensembl
Cytoband2q21.3
Allele length
AssemblyAllele length
hg38671
hg19671
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18255863
Samples
Known GenesZRANB3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538382
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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