A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6613



Internal ID15537250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:102602981..102625946hg38UCSC Ensembl
Outerchr14:103069318..103092283hg19UCSC Ensembl
Outerchr14:102139071..102162036hg18UCSC Ensembl
Outerchr14:102139071..102162036hg17UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3822966
hg1922966
hg1822966
hg1722966
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7257
Supporting Variants
SamplesNA12156
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)nssv6613
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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