A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1766



Internal ID15541049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:236348884..236390950hg38UCSC Ensembl
Outerchr1:236512184..236554250hg19UCSC Ensembl
Outerchr1:234578807..234620873hg18UCSC Ensembl
Outerchr1:232838225..232880291hg17UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg3842067
hg1942067
hg1842067
hg1742067
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4977
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)nssv1766
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