A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5543



Internal ID15543914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:27665785..27688696hg38UCSC Ensembl
Outerchr15:27910931..27933842hg19UCSC Ensembl
Outerchr15:25584526..25607437hg18UCSC Ensembl
Outerchr15:25584526..25607437hg17UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3822912
hg1922912
hg1822912
hg1722912
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1470
Supporting Variants
SamplesNA19129
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)nssv5543
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