A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3791



Internal ID15201750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:44797463..44832336hg38UCSC Ensembl
Outerchr3:44838955..44873828hg19UCSC Ensembl
Outerchr3:44813959..44848832hg18UCSC Ensembl
Outerchr3:44813959..44848832hg17UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg384872
hg194872
hg184872
hg174872
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3160
SamplesNA12878
Known GenesKIF15
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)nsv3791
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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