A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9282



Internal ID15540233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:17776842..17897019hg38UCSC Ensembl
Outerchr12:17929776..18049953hg19UCSC Ensembl
Outerchr12:17821043..17941220hg18UCSC Ensembl
Outerchr12:17821043..17941220hg17UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg38120178
hg19120178
hg18120178
hg17120178
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7229
Supporting Variants
SamplesNA18517
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)nssv9282
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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