A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3702



Internal ID15548338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:12256576..12301217hg38UCSC Ensembl
Outerchr3:12298075..12342716hg19UCSC Ensembl
Outerchr3:12273075..12317716hg18UCSC Ensembl
Outerchr3:12273075..12317716hg17UCSC Ensembl
Cytoband3p25.2
Allele length
AssemblyAllele length
hg3844642
hg1944642
hg1844642
hg1744642
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7772
SamplesNA12156
Known GenesPPARG
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)nsv3702
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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