A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4741



Internal ID15543237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:49253741..49312266hg38UCSC Ensembl
Outerchr4:49255758..49314283hg19UCSC Ensembl
Outerchr4:48950515..49009040hg18UCSC Ensembl
Outerchr4:49096686..49155211hg17UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg3858526
hg1958526
hg1858526
hg1758526
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7360
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)nssv4741
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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