A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3164



Internal ID15537892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:50897597..50934664hg38UCSC Ensembl
Outerchr3:50935028..50972095hg19UCSC Ensembl
Outerchr3:50902753..50947135hg18UCSC Ensembl
Outerchr3:50902753..50947135hg17UCSC Ensembl
Cytoband3p21.2
Allele length
AssemblyAllele length
hg3837068
hg1937068
hg1844383
hg1744383
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7353
Supporting Variants
SamplesNA12878
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)nssv3164
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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