A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953733



Internal ID17302607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:9380192..9403391hg38UCSC Ensembl
OuterchrY:9217801..9241000hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3823200
hg1923200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000346
SamplesBILGI_BIOE
Known GenesTSPY10, TSPY3, TSPY4
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953733
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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