A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1113015



Internal ID18919357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:126326621..126327121hg38UCSC Ensembl
Outerchr9:129088900..129089400hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38501
hg19501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4139n106
Supporting Variantsnssv3967901
SamplesKWS2
Known GenesMVB12B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1113015
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