A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv984



Internal ID15198225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:1894043..1977908hg38UCSC Ensembl
Outerchr11:1915273..1999138hg19UCSC Ensembl
Outerchr11:1871849..1955714hg18UCSC Ensembl
Outerchr11:1871849..1955714hg17UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3883866
hg1983866
hg1883866
hg1783866
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7213
Supporting Variants
SamplesNA19240
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)nssv984
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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