A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10480



Internal ID15195632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:158351995..158390195hg38UCSC Ensembl
Outerchr5:157779003..157817203hg19UCSC Ensembl
Outerchr5:157711581..157749781hg18UCSC Ensembl
Outerchr5:157711581..157749781hg17UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg3838201
hg1938201
hg1838201
hg1738201
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7372
Supporting Variants
SamplesNA18956
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)nssv10480
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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