A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6760



Internal ID15551702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:135644330..135673927hg38UCSC Ensembl
Outerchr9:138536176..138565773hg19UCSC Ensembl
Outerchr9:137675997..137705594hg18UCSC Ensembl
Outerchr9:135762121..135791718hg17UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg385016
hg195016
hg185016
hg175016
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3757
SamplesNA12878
Known GenesLCN9
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nsv6760
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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