A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2119



Internal ID15194716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:78910014..78940030hg38UCSC Ensembl
Outerchr15:79202356..79232372hg19UCSC Ensembl
Outerchr15:76989411..77019427hg18UCSC Ensembl
Outerchr15:76989411..77019427hg17UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3810006
hg1910006
hg1810006
hg1710006
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1629
Supporting Variants
SamplesNA18555
Known GenesCTSH
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)nssv2119
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