A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7257



Internal ID15552248
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 Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6613, nssv5524
SamplesNA12156, NA19129
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)nsv7257
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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