A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8982



Internal ID15534882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:130828615..130873569hg38UCSC Ensembl
Outerchr11:130698510..130743464hg19UCSC Ensembl
Outerchr11:130203720..130248674hg18UCSC Ensembl
Outerchr11:130203720..130248674hg17UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg3844955
hg1944955
hg1844955
hg1744955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551
Supporting Variants
SamplesNA12156
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)nssv8982
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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