A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2995782



Internal ID15776917
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 Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515229
Supporting Variants
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)nssv2995782
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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