A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2880



Internal ID15200757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:112959225..112979344hg38UCSC Ensembl
Outerchr2:113716802..113736921hg19UCSC Ensembl
Outerchr2:113433273..113453392hg18UCSC Ensembl
Outerchr2:113433033..113453152hg17UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg3820120
hg1920120
hg1820120
hg1720120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7541
SamplesNA12156
Known GenesIL36G
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)nsv2880
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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