A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730175



Internal ID21400986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:21063257..21065044hg38UCSC Ensembl
chrY:23225143..23226930hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg381788
hg191788
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16258268, nssv16256159
SamplesHG00731
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nsv4730175
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