A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1078153



Internal ID19317699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:7310858..7326359hg38UCSC Ensembl
chrY:7178899..7194400hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3815502
hg1915502
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3770049
SamplesKWP1
Known GenesPRKY
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1078153
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