A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730073



Internal ID21400889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:12951585..13252999hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38301415
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16257455, nssv16257443, nssv16256541, nssv16257895, nssv16258721, nssv16257224, nssv16258637, nssv16256726, nssv16257341, nssv16257772, nssv16255997, nssv16255965, nssv16258636, nssv16258227, nssv16258641, nssv16256896, nssv16257839, nssv16256524, nssv16256226, nssv16258191, nssv16258098, nssv16256255, nssv16258225, nssv16257495, nssv16257132, nssv16257290, nssv16256447, nssv16256043, nssv16256052, nssv16256007, nssv16258663, nssv16256663, nssv16256365, nssv16258605, nssv16257161, nssv16257385, nssv16257643
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nsv4730073
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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