A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730176



Internal ID21400987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:18765864..18845318hg38UCSC Ensembl
chr22:18753377..18832831hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3879455
hg1979455
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16256453, nssv16257995, nssv16256580
SamplesHG00731, HG00733
Known GenesGGT3P
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nsv4730176
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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