A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv832



Internal ID15552853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:50703550..50748439hg38UCSC Ensembl
Outerchr1:51169222..51214111hg19UCSC Ensembl
Outerchr1:50941810..50986699hg18UCSC Ensembl
Outerchr1:50881243..50926132hg17UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg3844890
hg1944890
hg1844890
hg1744890
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9118
SamplesNA12156
Known GenesFAF1
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)nsv832
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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