A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4166



Internal ID15538893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:78026369..78061638hg38UCSC Ensembl
Outerchr15:78318711..78353980hg19UCSC Ensembl
Outerchr15:76105766..76141035hg18UCSC Ensembl
Outerchr15:76105766..76141035hg17UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg384478
hg194478
hg184478
hg174478
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1626
Supporting Variants
SamplesNA12878
Known GenesTBC1D2B
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)nssv4166
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