A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10792



Internal ID15195320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:1884380..1918834hg38UCSC Ensembl
Outerchr11:1905610..1940064hg19UCSC Ensembl
Outerchr11:1862186..1896640hg18UCSC Ensembl
Outerchr11:1862186..1896640hg17UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3834455
hg1934455
hg1834455
hg1734455
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7213
Supporting Variants
SamplesNA18956
Known GenesLSP1
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)nssv10792
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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