A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7915



Internal ID15189263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:733398..774271hg38UCSC Ensembl
Outerchr4:727187..768059hg19UCSC Ensembl
Outerchr4:717187..758059hg18UCSC Ensembl
Outerchr4:717187..757889hg17UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3840874
hg1940873
hg1840873
hg1740703
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4195
Supporting Variants
SamplesNA12156
Known GenesPCGF3
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)nssv7915
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