A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2616



Internal ID15193811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:137473055..137505021hg38UCSC Ensembl
Outerchr6:137794192..137826158hg19UCSC Ensembl
Outerchr6:137835885..137867851hg18UCSC Ensembl
Outerchr6:137835885..137867851hg17UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg388062
hg198062
hg188062
hg178062
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5491
Supporting Variants
SamplesNA18555
Known GenesOLIG3
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)nssv2616
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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