A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8888



Internal ID15188290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:20632781..20677607hg38UCSC Ensembl
Outerchr11:20654327..20699153hg19UCSC Ensembl
Outerchr11:20610903..20655729hg18UCSC Ensembl
Outerchr11:20610903..20655729hg17UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3844827
hg1944827
hg1844827
hg1744827
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7703
Supporting Variants
SamplesNA12156
Known GenesNELL1, SLC6A5
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)nssv8888
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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