A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10111



Internal ID15542686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:12440523..12474868hg38UCSC Ensembl
Outerchr17:12343840..12378185hg19UCSC Ensembl
Outerchr17:12284565..12318910hg18UCSC Ensembl
Outerchr17:12284565..12318910hg17UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3834346
hg1934346
hg1834346
hg1734346
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1984
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)nssv10111
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