A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9841



Internal ID15539909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:80420176..80454445hg38UCSC Ensembl
Outerchr12:80813956..80854174hg19UCSC Ensembl
Outerchr12:79338087..79378305hg18UCSC Ensembl
Outerchr12:79316424..79356642hg17UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg3834270
hg1940219
hg1840219
hg1740219
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7231
Supporting Variants
SamplesNA18507
Known GenesPTPRQ
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)nssv9841
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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