A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1112483



Internal ID18908865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:103014750..103014806hg38UCSC Ensembl
Outerchr9:105777032..105777088hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4111n106
Supporting Variantsnssv3966573
SamplesKWS2
Known GenesCYLC2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1112483
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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