A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515229



Internal ID15813586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:24002589..24047849hg38UCSC Ensembl
InnerchrY:26148736..26193996hg19UCSC Ensembl
InnerchrY:24558124..24603384hg18UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg3845261
hg1945261
hg1845261
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2995782
SamplesNA21310
Known GenesCDY1, CDY1B
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nsv515229
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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