A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6602



Internal ID15551528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:88140078..88171305hg38UCSC Ensembl
Outerchr9:90754993..90786220hg19UCSC Ensembl
Outerchr9:89944813..89976040hg18UCSC Ensembl
Outerchr9:87984547..88015774hg17UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg389772
hg199772
hg189772
hg179772
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv816
SamplesNA19240
Known Genes
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)nsv6602
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