A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950512



Internal ID16952699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:135182463..135221062hg38UCSC Ensembl
Outerchr6:135503601..135542200hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg3838600
hg1938600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997523
SamplesBILGI_BIOE
Known GenesMYB
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950512
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