A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9511



Internal ID15539803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:23208288..23224031hg38UCSC Ensembl
Outerchr15:22649037..22664780hg19UCSC Ensembl
Outerchr15:20200401..20216144hg18UCSC Ensembl
Outerchr15:20200401..20216144hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3815744
hg1915744
hg1815744
hg1715744
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7260
Supporting Variants
SamplesNA18507
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)nssv9511
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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