A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3775



Internal ID15548418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:40616612..40648990hg38UCSC Ensembl
Outerchr3:40658103..40690481hg19UCSC Ensembl
Outerchr3:40633107..40665485hg18UCSC Ensembl
Outerchr3:40633107..40665485hg17UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg386874
hg196874
hg186874
hg176874
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5959
SamplesNA19129
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)nsv3775
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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