A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3806



Internal ID15201766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:47447294..47476643hg38UCSC Ensembl
Outerchr3:47488784..47518133hg19UCSC Ensembl
Outerchr3:47463788..47493137hg18UCSC Ensembl
Outerchr3:47463788..47493137hg17UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3829350
hg1929350
hg1829350
hg1729350
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2393
SamplesNA18555
Known GenesSCAP
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)nsv3806
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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