A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3254



Internal ID15537982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:49501919..49576768hg38UCSC Ensembl
Outerchr4:49503936..49578785hg19UCSC Ensembl
Outerchr4:49198693..49273542hg18UCSC Ensembl
Outerchr4:49344864..49419713hg17UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg3874850
hg1974850
hg1874850
hg1774850
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7361
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)nssv3254
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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