A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9381



Internal ID15540332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:50897597..50936002hg38UCSC Ensembl
Outerchr3:50935028..50973433hg19UCSC Ensembl
Outerchr3:50903944..50948473hg18UCSC Ensembl
Outerchr3:50903944..50948473hg17UCSC Ensembl
Cytoband3p21.2
Allele length
AssemblyAllele length
hg3838406
hg1938406
hg1844530
hg1744530
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7353
Supporting Variants
SamplesNA18517
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)nssv9381
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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