A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5538



Internal ID15543921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:23194406..23226214hg38UCSC Ensembl
Outerchr15:22646854..22678662hg19UCSC Ensembl
Outerchr15:20198218..20230026hg18UCSC Ensembl
Outerchr15:20198218..20230026hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3831809
hg1931809
hg1831809
hg1731809
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7260
Supporting Variants
SamplesNA19129
Known GenesMIR4509-1, MIR4509-2, MIR4509-3
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)nssv5538
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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