A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6435



Internal ID15190743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:1867726..1916670hg38UCSC Ensembl
Outerchr11:1888956..1937900hg19UCSC Ensembl
Outerchr11:1845532..1894476hg18UCSC Ensembl
Outerchr11:1845532..1894476hg17UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3848945
hg1948945
hg1848945
hg1748945
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7643
Supporting Variants
SamplesNA12156
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)nssv6435
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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