A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5490



Internal ID15203619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:135164564..135198488hg38UCSC Ensembl
Outerchr6:135485702..135519626hg19UCSC Ensembl
Outerchr6:135527395..135561319hg18UCSC Ensembl
Outerchr6:135527395..135561319hg17UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg385513
hg195513
hg185513
hg175513
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8300
SamplesNA12156
Known GenesMYB
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)nsv5490
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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