A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1150373



Internal ID18851601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:106709699..106709757hg38UCSC Ensembl
Outerchr11:106580425..106580483hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4003675
SamplesKWB1
Known GenesGUCY1A2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1150373
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