A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9960



Internal ID15193367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:77034510..77050067hg38UCSC Ensembl
Outerchr15:77326851..77342409hg19UCSC Ensembl
Outerchr15:75113906..75129464hg18UCSC Ensembl
Outerchr15:75113906..75129464hg17UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg387779
hg197779
hg187779
hg177779
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1622
Supporting Variants
SamplesNA18507
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)nssv9960
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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