A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1150365



Internal ID18854370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:57340801..57374302hg38UCSC Ensembl
Outerchr6:57205599..57239100hg19UCSC Ensembl
Cytoband6p11.2
Allele length
AssemblyAllele length
hg3833502
hg1933502
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4003666
SamplesKWB1
Known GenesPRIM2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1150365
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