A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5524



Internal ID15543937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:102602914..102629834hg38UCSC Ensembl
Outerchr14:103069251..103096171hg19UCSC Ensembl
Outerchr14:102139004..102165924hg18UCSC Ensembl
Outerchr14:102139004..102165924hg17UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3826921
hg1926921
hg1826921
hg1726921
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7257
Supporting Variants
SamplesNA19129
Known GenesRCOR1
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)nssv5524
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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