A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1540



Internal ID15545538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:138246815..138290613hg38UCSC Ensembl
Outerchr2:139004385..139048183hg19UCSC Ensembl
Outerchr2:138720855..138764653hg18UCSC Ensembl
Outerchr2:138838117..138881915hg17UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg3843799
hg1943799
hg1843799
hg1743799
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7330
Supporting Variants
SamplesNA19240
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)nssv1540
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