A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6669



Internal ID15204915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:112437999..112471024hg38UCSC Ensembl
Outerchr9:115200279..115233304hg19UCSC Ensembl
Outerchr9:114240100..114273125hg18UCSC Ensembl
Outerchr9:112279834..112312859hg17UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg386718
hg196718
hg186718
hg176718
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3741
SamplesNA12878
Known GenesHSDL2
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)nsv6669
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