A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3420



Internal ID15191462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:22162923..22197800hg38UCSC Ensembl
Outerchr6:22163152..22198029hg19UCSC Ensembl
Outerchr6:22271131..22306008hg18UCSC Ensembl
Outerchr6:22271131..22306008hg17UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg384874
hg194874
hg184874
hg174874
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5224
Supporting Variants
SamplesNA12878
Known GenesCASC15
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)nssv3420
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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