A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9828



Internal ID15193207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:9252404..9441490hg38UCSC Ensembl
Outerchr12:9405000..9594086hg19UCSC Ensembl
Outerchr12:9296267..9485353hg18UCSC Ensembl
Outerchr12:9296267..9485353hg17UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38189087
hg19189087
hg18189087
hg17189087
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7228
Supporting Variants
SamplesNA18507
Known GenesDDX12P, LOC642846
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)nssv9828
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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