A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10875



Internal ID15541923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:80461952..80503303hg38UCSC Ensembl
Outerchr12:80848593..80897082hg19UCSC Ensembl
Outerchr12:79372724..79421213hg18UCSC Ensembl
Outerchr12:79351061..79399550hg17UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg3841352
hg1948490
hg1848490
hg1748490
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7231
Supporting Variants
SamplesNA18956
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)nssv10875
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer