A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10853



Internal ID15541945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:17744777..17846188hg38UCSC Ensembl
Outerchr12:17897711..17999122hg19UCSC Ensembl
Outerchr12:17788978..17890389hg18UCSC Ensembl
Outerchr12:17788978..17890389hg17UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg38101412
hg19101412
hg18101412
hg17101412
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7229
Supporting Variants
SamplesNA18956
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)nssv10853
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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