A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5408



Internal ID15544012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:17773810..17895073hg38UCSC Ensembl
Outerchr12:17926744..18048007hg19UCSC Ensembl
Outerchr12:17818011..17939274hg18UCSC Ensembl
Outerchr12:17818011..17939274hg17UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg38121264
hg19121264
hg18121264
hg17121264
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7229
Supporting Variants
SamplesNA19129
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)nssv5408
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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