A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9288



Internal ID15540239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:108083183..108106030hg38UCSC Ensembl
Outerchr12:108476960..108499807hg19UCSC Ensembl
Outerchr12:107001090..107023937hg18UCSC Ensembl
Outerchr12:106979427..107002274hg17UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg3822848
hg1922848
hg1822848
hg1722848
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7235
Supporting Variants
SamplesNA18517
Known Genes
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)nssv9288
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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