A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515231



Internal ID15466863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:24907965..26020889hg38UCSC Ensembl
InnerchrY:27054112..28167036hg19UCSC Ensembl
InnerchrY:25463500..26576424hg18UCSC Ensembl
CytobandYq11.23
Allele length
AssemblyAllele length
hg381112925
hg191112925
hg181112925
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2995784
SamplesNA21310
Known GenesBPY2, BPY2B, BPY2C, CDY1, CDY1B, CSPG4P1Y, GOLGA2P2Y, GOLGA2P3Y, TTTY17A, TTTY17B, TTTY17C, TTTY3, TTTY3B, TTTY4, TTTY4B, TTTY4C
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nsv515231
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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