A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10289



Internal ID15542509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:25866240..26026147hg38UCSC Ensembl
Outerchr20:25846876..26006783hg19UCSC Ensembl
Outerchr20:25794876..25954783hg18UCSC Ensembl
Outerchr20:25794876..25954783hg17UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg38159908
hg19159908
hg18159908
hg17159908
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7340
Supporting Variants
SamplesNA18956
Known GenesLOC100134868
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)nssv10289
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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