A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730216



Internal ID21401027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:23463146..23716571hg38UCSC Ensembl
chrY:25609293..25862718hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg38253426
hg19253426
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16257029, nssv16258318
SamplesHG00512, NA19239
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nsv4730216
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