A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2113



Internal ID15541396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:68470847..68504018hg38UCSC Ensembl
Outerchr15:68763186..68796357hg19UCSC Ensembl
Outerchr15:66550240..66583411hg18UCSC Ensembl
Outerchr15:66550240..66583411hg17UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg386848
hg196848
hg186848
hg176848
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1583
Supporting Variants
SamplesNA18555
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)nssv2113
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