A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730259



Internal ID21401070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:17863396..18408694hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38545299
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16256782, nssv16257742, nssv16256055, nssv16257182, nssv16257755, nssv16258681, nssv16258067, nssv16256105, nssv16257533, nssv16257086, nssv16256821, nssv16255867, nssv16258886, nssv16257052, nssv16258096, nssv16257904, nssv16257528, nssv16256054, nssv16256646, nssv16257356, nssv16255891, nssv16256513, nssv16256448, nssv16255900, nssv16257762, nssv16256514, nssv16256941, nssv16257806
SamplesNA19238, NA19239, HG00732, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nsv4730259
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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