A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4147



Internal ID15192188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:40617206..40624036hg38UCSC Ensembl
Outerchr15:40909404..40916234hg19UCSC Ensembl
Outerchr15:38696696..38703526hg18UCSC Ensembl
Outerchr15:38696696..38703526hg17UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg386831
hg196831
hg186831
hg176831
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7263
Supporting Variants
SamplesNA12878
Known GenesCASC5
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)nssv4147
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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