A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7414



Internal ID15189764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:74069344..74114064hg38UCSC Ensembl
Outerchr18:71736579..71781299hg19UCSC Ensembl
Outerchr18:69887559..69932279hg18UCSC Ensembl
Outerchr18:69887559..69932279hg17UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3844721
hg1944721
hg1844721
hg1744721
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2355
Supporting Variants
SamplesNA12156
Known GenesFBXO15
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)nssv7414
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