A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5375



Internal ID15543047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:101693581..101706256hg38UCSC Ensembl
Outerchr11:101564312..101576987hg19UCSC Ensembl
Outerchr11:101069522..101082197hg18UCSC Ensembl
Outerchr11:101069522..101082197hg17UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3812676
hg1912676
hg1812676
hg1712676
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv461
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)nssv5375
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