A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10343



Internal ID15542455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:50887802..50936759hg38UCSC Ensembl
Outerchr3:50925233..50974190hg19UCSC Ensembl
Outerchr3:50900252..50949230hg18UCSC Ensembl
Outerchr3:50900252..50949230hg17UCSC Ensembl
Cytoband3p21.2
Allele length
AssemblyAllele length
hg3848958
hg1948958
hg1848979
hg1748979
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)nssv10343
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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