A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1250



Internal ID15197790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:44823214..45039390hg38UCSC Ensembl
Outerchr15:45115412..45331588hg19UCSC Ensembl
Outerchr15:42902704..43118880hg18UCSC Ensembl
Outerchr15:42902704..43118880hg17UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38216177
hg19216177
hg18216177
hg17216177
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7264
Supporting Variants
SamplesNA19240
Known GenesC15orf43, SORD
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)nssv1250
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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