A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4353



Internal ID15192394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:33294939..33313582hg38UCSC Ensembl
Outerchr19:33785845..33804488hg19UCSC Ensembl
Outerchr19:38477685..38496328hg18UCSC Ensembl
Outerchr19:38477685..38496328hg17UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3818644
hg1918644
hg1818644
hg1718644
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2463
Supporting Variants
SamplesNA12878
Known GenesCEBPA, CEBPA-AS1
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)nssv4353
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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