A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6473



Internal ID15537391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:89884120..89912789hg38UCSC Ensembl
Outerchr11:89617288..89645957hg19UCSC Ensembl
Outerchr11:89256936..89285605hg18UCSC Ensembl
Outerchr11:89256936..89285605hg17UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3828670
hg1928670
hg1828670
hg1728670
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7222
Supporting Variants
SamplesNA12156
Known GenesMIR5692A1, TRIM49D1, TRIM49D2P
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)nssv6473
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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