A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257423



Internal ID21398062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:22168036..22637147hg38UCSC Ensembl
chrY:24314183..24783294hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg38469112
hg19469112
Variant TypeOTHER inversion
Copy Number
Allele StateHemizygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730228
Supporting Variants
SamplesHG00512
Known GenesLOC100652931, PRY, PRY2, RBMY1F, RBMY1J, RBMY2FP, TTTY5, TTTY6, TTTY6B
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257423
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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