A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14102212



Internal ID21269149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:22215341..22739725hg38UCSC Ensembl
InnerchrY:24361488..24885872hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg38524385
hg19524385
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111880
Supporting Variants
Samplessample136
Known GenesLOC100652931, PRY, PRY2, RBMY1F, RBMY1J, RBMY2FP, TTTY5, TTTY6, TTTY6B
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14102212
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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