A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4589



Internal ID15549313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:164608715..164653545hg38UCSC Ensembl
Outerchr4:165529867..165574697hg19UCSC Ensembl
Outerchr4:165749317..165794147hg18UCSC Ensembl
Outerchr4:165887472..165932302hg17UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3844831
hg1944831
hg1844831
hg1744831
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8024
SamplesNA12156
Known GenesMIR5684
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)nsv4589
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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