A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730114



Internal ID21400925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:29869823..30424993hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38555171
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16257380, nssv16255888, nssv16258619, nssv16258018, nssv16256227, nssv16258611, nssv16258133, nssv16256781, nssv16257463, nssv16258263, nssv16256068, nssv16256012, nssv16257079, nssv16257127, nssv16258291, nssv16256577, nssv16258310, nssv16257951, nssv16258741, nssv16258468, nssv16256256, nssv16258368, nssv16257623, nssv16256735
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nsv4730114
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer