A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1447



Internal ID15544259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:29878718..29904640hg38UCSC Ensembl
Outerchr19:30369625..30395547hg19UCSC Ensembl
Outerchr19:35061465..35087387hg18UCSC Ensembl
Outerchr19:35061465..35087387hg17UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3825923
hg1925923
hg1825923
hg1725923
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv2457
Supporting Variants
SamplesNA19240
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)nssv1447
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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