A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1078154



Internal ID19326111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:10112190..10125091hg38UCSC Ensembl
chrY:9949799..9962700hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3812902
hg1912902
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3771480
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1078154
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