A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1111170



Internal ID18914492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:35116772..35116825hg38UCSC Ensembl
Outerchr19:35607676..35607729hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1773n106
Supporting Variantsnssv3962418
SamplesKWS1
Known GenesFXYD3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1111170
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