A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3109



Internal ID15540866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:147341576..147375627hg38UCSC Ensembl
Outerchr3:147059363..147093414hg19UCSC Ensembl
Outerchr3:148542053..148576104hg18UCSC Ensembl
Outerchr3:148542061..148576112hg17UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg385972
hg195972
hg185972
hg175972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4048
Supporting Variants
SamplesNA18555
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)nssv3109
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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