A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3208



Internal ID15537936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:151659660..151674445hg38UCSC Ensembl
Outerchr3:151377448..151392233hg19UCSC Ensembl
Outerchr3:152860138..152874923hg18UCSC Ensembl
Outerchr3:152860146..152874931hg17UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg389772
hg199772
hg189772
hg179772
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv4066
Supporting Variants
SamplesNA12878
Known GenesMIR548H2
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)nssv3208
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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