A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953716



Internal ID17302590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:378066..435365hg38UCSC Ensembl
OuterchrY:288801..346100hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg3857300
hg1957300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000329
SamplesBILGI_BIOE
Known GenesPPP2R3B
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953716
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer