A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4540



Internal ID15539267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:47868931..47893946hg38UCSC Ensembl
Outerchr20:46497675..46522690hg19UCSC Ensembl
Outerchr20:45931082..45956097hg18UCSC Ensembl
Outerchr20:45931082..45956097hg17UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg3825016
hg1925016
hg1825016
hg1725016
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7344
Supporting Variants
SamplesNA12878
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)nssv4540
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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