A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3189



Internal ID15537917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:109372352..109399470hg38UCSC Ensembl
Outerchr3:109091199..109118317hg19UCSC Ensembl
Outerchr3:110573889..110601007hg18UCSC Ensembl
Outerchr3:110573889..110601007hg17UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg3812632
hg1912632
hg1812632
hg1712632
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3939
Supporting Variants
SamplesNA12878
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)nssv3189
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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