A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10901



Internal ID15539489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:17739217..17849853hg38UCSC Ensembl
Outerchr12:17892151..18002787hg19UCSC Ensembl
Outerchr12:17783418..17894054hg18UCSC Ensembl
Outerchr12:17783418..17894054hg17UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg38110637
hg19110637
hg18110637
hg17110637
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7229
Supporting Variants
SamplesNA15510
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)nssv10901
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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