A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730145



Internal ID21400956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:20060965..20085126hg38UCSC Ensembl
chrY:22222851..22247012hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg3824162
hg1924162
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16258185, nssv16256538, nssv16258624, nssv16256930, nssv16257577
SamplesHG00512, NA19239, HG00731
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nsv4730145
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