A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3118027



Internal ID21301293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:22214711..23979146hg38UCSC Ensembl
InnerchrY:24360858..26125293hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg381764436
hg191764436
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14102274
Samplessample320
Known GenesBPY2, BPY2B, BPY2C, DAZ1, DAZ2, DAZ3, DAZ4, LOC100652931, PRY, PRY2, RBMY1F, RBMY1J, RBMY2FP, TTTY17A, TTTY17B, TTTY17C, TTTY3, TTTY3B, TTTY4, TTTY4B, TTTY4C, TTTY5, TTTY6, TTTY6B
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3118027
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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