A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11017



Internal ID15193005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:95432430..95686232hg38UCSC Ensembl
Outerchr2:96098178..96351980hg19UCSC Ensembl
Outerchr2:95461905..95715707hg18UCSC Ensembl
Outerchr2:95520052..95773854hg17UCSC Ensembl
Cytoband2q11.1
Allele length
AssemblyAllele length
hg38253803
hg19253803
hg18253803
hg17253803
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7320
Supporting Variants
SamplesNA15510
Known GenesTRIM43, TRIM43B
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)nssv11017
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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