A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3421



Internal ID15191463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:24798895..24819309hg38UCSC Ensembl
Outerchr6:24799123..24819537hg19UCSC Ensembl
Outerchr6:24907102..24927516hg18UCSC Ensembl
Outerchr6:24907102..24927516hg17UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg3820415
hg1920415
hg1820415
hg1720415
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5227
Supporting Variants
SamplesNA12878
Known GenesFAM65B, LOC101928603
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)nssv3421
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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