A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3752



Internal ID15548393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:32546740..32556434hg38UCSC Ensembl
Outerchr3:32588232..32597926hg19UCSC Ensembl
Outerchr3:32563236..32572930hg18UCSC Ensembl
Outerchr3:32563236..32572930hg17UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg389695
hg199695
hg189695
hg179695
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7786
SamplesNA12156
Known GenesDYNC1LI1
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)nsv3752
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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