A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4365



Internal ID15539092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:46089618..46113501hg38UCSC Ensembl
Outerchr19:46592876..46616759hg19UCSC Ensembl
Outerchr19:51284716..51308599hg18UCSC Ensembl
Outerchr19:51284716..51308599hg17UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3823884
hg1923884
hg1823884
hg1723884
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv2510
Supporting Variants
SamplesNA12878
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)nssv4365
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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