A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110698



Internal ID19285877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:109498649..109498710hg38UCSC Ensembl
Outerchr13:110150996..110151057hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3961106
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110698
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer