A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv356



Internal ID15544744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:187418205..187466062hg38UCSC Ensembl
Outerchr3:187135993..187183850hg19UCSC Ensembl
Outerchr3:188618687..188666544hg18UCSC Ensembl
Outerchr3:188618695..188666552hg17UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg3847858
hg1947858
hg1847858
hg1747858
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7357
Supporting Variants
SamplesNA19240
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)nssv356
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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