A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5907



Internal ID15543474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:41767915..41789940hg38UCSC Ensembl
Outerchr21:43188075..43210100hg19UCSC Ensembl
Outerchr21:42061144..42083169hg18UCSC Ensembl
Outerchr21:42061144..42083169hg17UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3822026
hg1922026
hg1822026
hg1722026
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7348
Supporting Variants
SamplesNA19129
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)nssv5907
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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