A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1125030



Internal ID18918216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:40275482..40341082hg38UCSC Ensembl
Outerchr9:42420500..42486100hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3865601
hg1965601
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3977835
SamplesKWS2
Known GenesFAM95B1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1125030
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