A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1266



Internal ID15197772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:77033568..77049247hg38UCSC Ensembl
Outerchr15:77325909..77341589hg19UCSC Ensembl
Outerchr15:75112964..75128644hg18UCSC Ensembl
Outerchr15:75112964..75128644hg17UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg386408
hg196408
hg186408
hg176408
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1622
Supporting Variants
SamplesNA19240
Known GenesPSTPIP1, TSPAN3
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)nssv1266
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