A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3917



Internal ID15191958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:1896639..1974771hg38UCSC Ensembl
Outerchr11:1917869..1996001hg19UCSC Ensembl
Outerchr11:1874445..1952577hg18UCSC Ensembl
Outerchr11:1874445..1952577hg17UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3878133
hg1978133
hg1878133
hg1778133
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7213
Supporting Variants
SamplesNA12878
Known GenesMRPL23, TNNT3
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)nssv3917
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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