A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3704



Internal ID15548340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:13134106..13165700hg38UCSC Ensembl
Outerchr3:13175606..13207200hg19UCSC Ensembl
Outerchr3:13150606..13182200hg18UCSC Ensembl
Outerchr3:13150606..13182200hg17UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg389392
hg199392
hg189392
hg179392
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1656
SamplesNA19240
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)nsv3704
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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