A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9273



Internal ID15540224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:89863911..90012421hg38UCSC Ensembl
Outerchr11:89597079..89745589hg19UCSC Ensembl
Outerchr11:89236727..89385237hg18UCSC Ensembl
Outerchr11:89236727..89385237hg17UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38148511
hg19148511
hg18148511
hg17148511
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7222
Supporting Variants
SamplesNA18517
Known GenesMIR5692A1, TRIM49D1, TRIM49D2P, TRIM53AP, TRIM64, TRIM64B
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)nssv9273
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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