A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1029



Internal ID15545146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:93414865..93438516hg38UCSC Ensembl
Outerchr11:93148031..93171682hg19UCSC Ensembl
Outerchr11:92787679..92811330hg18UCSC Ensembl
Outerchr11:92787679..92811330hg17UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3823652
hg1923652
hg1823652
hg1723652
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv439
Supporting Variants
SamplesNA19240
Known GenesCCDC67
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)nssv1029
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