A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2464



Internal ID15540664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:49255587..49315342hg38UCSC Ensembl
Outerchr4:49257604..49317359hg19UCSC Ensembl
Outerchr4:48952361..49012116hg18UCSC Ensembl
Outerchr4:49098532..49158287hg17UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg3859756
hg1959756
hg1859756
hg1759756
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7360
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)nssv2464
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer