A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3857



Internal ID15548508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:65715948..65746459hg38UCSC Ensembl
Outerchr3:65701623..65732134hg19UCSC Ensembl
Outerchr3:65676663..65707174hg18UCSC Ensembl
Outerchr3:65676663..65707174hg17UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg389516
hg199516
hg189516
hg179516
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2398
SamplesNA18555
Known GenesMAGI1
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)nsv3857
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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