A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2335



Internal ID15540806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:47862383..47899155hg38UCSC Ensembl
Outerchr20:46491127..46527899hg19UCSC Ensembl
Outerchr20:45924534..45961306hg18UCSC Ensembl
Outerchr20:45924534..45961306hg17UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg3836773
hg1936773
hg1836773
hg1736773
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7344
Supporting Variants
SamplesNA18555
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)nssv2335
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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