A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3675



Internal ID15201622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:2994648..3039460hg38UCSC Ensembl
Outerchr3:3036332..3081144hg19UCSC Ensembl
Outerchr3:3011332..3056144hg18UCSC Ensembl
Outerchr3:3011332..3056144hg17UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg3844813
hg1944813
hg1844813
hg1744813
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7765
SamplesNA12156
Known GenesCNTN4
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)nsv3675
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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