A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7681



Internal ID15206029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:11860698..11905567hg38UCSC Ensembl
Outerchr11:11882245..11927114hg19UCSC Ensembl
Outerchr11:11838821..11883690hg18UCSC Ensembl
Outerchr11:11838821..11883690hg17UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg3844870
hg1944870
hg1844870
hg1744870
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8882
SamplesNA12156
Known GenesUSP47
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)nsv7681
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