A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1077515



Internal ID19317101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:11025689..11027290hg38UCSC Ensembl
chr8:10883199..10884800hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg381602
hg191602
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3772511
SamplesKWP1
Known GenesXKR6
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1077515
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