A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730227



Internal ID21401038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:14019590..14049366hg38UCSC Ensembl
chrY:16131470..16161246hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg3829777
hg1929777
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16258068, nssv16258577, nssv16257464, nssv16258831
SamplesNA19239, HG00731
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nsv4730227
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