A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7264



Internal ID15205570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:44822196..45121630hg38UCSC Ensembl
Outerchr15:45114394..45413828hg19UCSC Ensembl
Outerchr15:42901686..43201120hg18UCSC Ensembl
Outerchr15:42901686..43201120hg17UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38299435
hg19299435
hg18299435
hg17299435
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1250, nssv9309
SamplesNA18517, NA19240
Known GenesC15orf43, DUOX2, DUOXA1, DUOXA2, SORD
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)nsv7264
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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