A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1132723



Internal ID19278783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:67842171..67847242hg38UCSC Ensembl
Outerchr9:67909500..67914800hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg385072
hg195301
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3987513
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1132723
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