A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3691



Internal ID15548326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:9301454..9346104hg38UCSC Ensembl
Outerchr3:9343138..9387788hg19UCSC Ensembl
Outerchr3:9318138..9362788hg18UCSC Ensembl
Outerchr3:9318138..9362788hg17UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3844651
hg1944651
hg1844651
hg1744651
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7769
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)nsv3691
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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