A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3749



Internal ID15191791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:123938573..123991662hg38UCSC Ensembl
Outerchr9:126700852..126753941hg19UCSC Ensembl
Outerchr9:125740673..125793762hg18UCSC Ensembl
Outerchr9:123780406..123833495hg17UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3853090
hg1953090
hg1853090
hg1753090
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7435
Supporting Variants
SamplesNA12878
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)nssv3749
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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