A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11154



Internal ID15539425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:97756261..97793986hg38UCSC Ensembl
Outerchr7:97385573..97423298hg19UCSC Ensembl
Outerchr7:97223509..97261234hg18UCSC Ensembl
Outerchr7:97030224..97067949hg17UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3837726
hg1937726
hg1837726
hg1737726
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5858
Supporting Variants
SamplesNA15510
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)nssv11154
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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