A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5213



Internal ID15197343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:13004739..13111433hg38UCSC Ensembl
Outerchr1:13142403..13178905hg19UCSC Ensembl
Outerchr1:13064990..13101492hg18UCSC Ensembl
Outerchr1:12966386..13002888hg17UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg38106695
hg1936503
hg1836503
hg1736503
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7172
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)nssv5213
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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