A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4089



Internal ID15548763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:160567060..160612236hg38UCSC Ensembl
Outerchr3:160284848..160330024hg19UCSC Ensembl
Outerchr3:161767542..161812718hg18UCSC Ensembl
Outerchr3:161767550..161812726hg17UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg3845177
hg1945177
hg1845177
hg1745177
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7891
SamplesNA12156
Known Genes
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)nsv4089
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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