A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1232



Internal ID15544496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:20042576..20267466hg38UCSC Ensembl
Outerchr15:20247829..20472719hg19UCSC Ensembl
Outerchr15:18507843..18732733hg18UCSC Ensembl
Outerchr15:18507843..18732733hg17UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38224891
hg19224891
hg18224891
hg17224891
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7260
Supporting Variants
SamplesNA19240
Known Genes
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)nssv1232
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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