A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7267



Internal ID8519241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:72330841..72362354hg38UCSC Ensembl
Outerchr15:72623182..72654695hg19UCSC Ensembl
Outerchr15:70410236..70441749hg18UCSC Ensembl
Outerchr15:70410236..70441749hg17UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3831514
hg1931514
hg1831514
hg1731514
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1262
SamplesNA19240
Known GenesHEXA
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)nsv7267
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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