A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11059



Internal ID15539649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:50887801..50937800hg38UCSC Ensembl
Outerchr3:50925232..50975231hg19UCSC Ensembl
Outerchr3:50900251..50950271hg18UCSC Ensembl
Outerchr3:50900251..50950271hg17UCSC Ensembl
Cytoband3p21.2
Allele length
AssemblyAllele length
hg3850000
hg1950000
hg1850021
hg1750021
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7353
Supporting Variants
SamplesNA15510
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)nssv11059
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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