A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730228



Internal ID21401039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:21899633..22637147hg38UCSC Ensembl
chrY:24045780..24783294hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg38737515
hg19737515
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16258083, nssv16257423
SamplesHG00512
Known GenesLOC100652931, PRY, PRY2, RBMY1B, RBMY1D, RBMY1E, RBMY1F, RBMY1J, RBMY2FP, TTTY5, TTTY6, TTTY6B
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nsv4730228
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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