A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2413



Internal ID15200290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:9744152..9770775hg38UCSC Ensembl
Outerchr19:9854828..9881451hg19UCSC Ensembl
Outerchr19:9715828..9742451hg18UCSC Ensembl
Outerchr19:9715828..9742451hg17UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3826624
hg1926624
hg1826624
hg1726624
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5726
SamplesNA19129
Known GenesZNF846
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)nsv2413
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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