A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2411



Internal ID15200288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:9157073..9202645hg38UCSC Ensembl
Outerchr19:9267749..9313321hg19UCSC Ensembl
Outerchr19:9128749..9174321hg18UCSC Ensembl
Outerchr19:9128749..9174321hg17UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3845573
hg1945573
hg1845573
hg1745573
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1434, nssv2210
SamplesNA19240, NA18555
Known GenesOR7D2, ZNF317
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)nsv2411
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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