A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11204



Internal ID15192689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:123942952..123986101hg38UCSC Ensembl
Outerchr9:126705231..126748380hg19UCSC Ensembl
Outerchr9:125745052..125788201hg18UCSC Ensembl
Outerchr9:123784785..123827934hg17UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3843150
hg1943150
hg1843150
hg1743150
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7435
Supporting Variants
SamplesNA15510
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)nssv11204
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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