A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515232



Internal ID15813589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:26207417..26265061hg38UCSC Ensembl
InnerchrY:28353564..28411208hg19UCSC Ensembl
InnerchrY:26762952..26820596hg18UCSC Ensembl
CytobandYq11.23
Allele length
AssemblyAllele length
hg3857645
hg1957645
hg1857645
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2995785
SamplesNA21310
Known Genes
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nsv515232
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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