A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3869



Internal ID15548521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:70834807..70853943hg38UCSC Ensembl
Outerchr3:70883958..70903094hg19UCSC Ensembl
Outerchr3:70966648..70985784hg18UCSC Ensembl
Outerchr3:70966648..70985784hg17UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg3819137
hg1919137
hg1819137
hg1719137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7824
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)nsv3869
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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