A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6220



Internal ID15537643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:48216901..48269114hg19UCSC Ensembl
Outerchr8:48379454..48431667hg18UCSC Ensembl
Outerchr8:48379454..48431667hg17UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg1952214
hg1852214
hg1752214
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7416
Supporting Variants
SamplesNA12156
Known GenesSPIDR
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)nssv6220
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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