A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730128



Internal ID21400939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:149578220..149788478hg38UCSC Ensembl
chrX:148659876..148870140hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38210259
hg19210265
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16257912, nssv16258383, nssv16256102, nssv16257474, nssv16257994, nssv16256037, nssv16258744, nssv16257487, nssv16256913, nssv16258811, nssv16258526, nssv16257852, nssv16258773, nssv16256452, nssv16257604, nssv16258482, nssv16257477, nssv16258748, nssv16256848, nssv16257763, nssv16257362, nssv16258409, nssv16258474, nssv16256531, nssv16256185, nssv16257266, nssv16258295, nssv16257966, nssv16257802, nssv16258323, nssv16257251, nssv16258060, nssv16256477, nssv16258434, nssv16257501, nssv16257845, nssv16256021, nssv16256569, nssv16257301, nssv16257252, nssv16257677, nssv16257732, nssv16256653, nssv16258143, nssv16257915, nssv16258349, nssv16256219, nssv16256162, nssv16258646, nssv16257807
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesHSFX1, HSFX2, MAGEA11, MAGEA9, MAGEA9B, TMEM185A
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nsv4730128
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