A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1239



Internal ID15544488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:23206783..23214089hg38UCSC Ensembl
Outerchr15:22658979..22666285hg19UCSC Ensembl
Outerchr15:20210343..20217649hg18UCSC Ensembl
Outerchr15:20210343..20217649hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg387307
hg197307
hg187307
hg177307
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)nssv1239
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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