A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2882



Internal ID15200759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:113695137..113729107hg38UCSC Ensembl
Outerchr2:114452714..114486684hg19UCSC Ensembl
Outerchr2:114169184..114203154hg18UCSC Ensembl
Outerchr2:114168944..114202914hg17UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg385468
hg195468
hg185468
hg175468
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7542
SamplesNA12156
Known GenesMIR4782, SLC35F5
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)nsv2882
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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