A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5437



Internal ID15550246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:109801369..109834789hg38UCSC Ensembl
Outerchr6:110122572..110155992hg19UCSC Ensembl
Outerchr6:110229265..110262685hg18UCSC Ensembl
Outerchr6:110229265..110262685hg17UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg386296
hg196296
hg186296
hg176296
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3466
SamplesNA12878
Known GenesFIG4
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)nsv5437
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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