A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10054



Internal ID15542743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:54923829..54936233hg38UCSC Ensembl
Outerchr15:55216027..55228431hg19UCSC Ensembl
Outerchr15:53003319..53015723hg18UCSC Ensembl
Outerchr15:53003319..53015723hg17UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3812405
hg1912405
hg1812405
hg1712405
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1541
Supporting Variants
SamplesNA18956
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)nssv10054
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer