A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10342



Internal ID15542456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:50848004..50887906hg38UCSC Ensembl
Outerchr3:50885435..50925337hg19UCSC Ensembl
Outerchr3:50860439..50909642hg18UCSC Ensembl
Outerchr3:50860439..50909642hg17UCSC Ensembl
Cytoband3p21.2
Allele length
AssemblyAllele length
hg3839903
hg1939903
hg1849204
hg1749204
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7353
Supporting Variants
SamplesNA18956
Known GenesDOCK3
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)nssv10342
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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