A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3868



Internal ID15548520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:70702203..70726930hg38UCSC Ensembl
Outerchr3:70751354..70776081hg19UCSC Ensembl
Outerchr3:70834044..70858771hg18UCSC Ensembl
Outerchr3:70834044..70858771hg17UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg386670
hg196670
hg186670
hg176670
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10349, nssv3098
SamplesNA18956, NA18555
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)nsv3868
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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