A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2451



Internal ID15547014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:29086908..29114197hg38UCSC Ensembl
Outerchr19:29577815..29605104hg19UCSC Ensembl
Outerchr19:34269655..34296944hg18UCSC Ensembl
Outerchr19:34269655..34296944hg17UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3827290
hg1927290
hg1827290
hg1727290
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7433
SamplesNA12156
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)nsv2451
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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