A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3733



Internal ID15201686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:24175086..24220258hg38UCSC Ensembl
Outerchr3:24216577..24261749hg19UCSC Ensembl
Outerchr3:24191581..24236753hg18UCSC Ensembl
Outerchr3:24191581..24236753hg17UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg3845173
hg1945173
hg1845173
hg1745173
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7780
SamplesNA12156
Known GenesTHRB
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)nsv3733
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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