A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4234



Internal ID15202237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:10511797..10545696hg38UCSC Ensembl
Outerchr4:10513421..10547320hg19UCSC Ensembl
Outerchr4:10122519..10156418hg18UCSC Ensembl
Outerchr4:10189690..10223589hg17UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg385532
hg195532
hg185532
hg175532
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7924
SamplesNA12156
Known GenesCLNK
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)nsv4234
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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