A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11120



Internal ID15539459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:18032114..18063686hg38UCSC Ensembl
Outerchr6:18032345..18063917hg19UCSC Ensembl
Outerchr6:18140324..18171896hg18UCSC Ensembl
Outerchr6:18140324..18171896hg17UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg388308
hg198308
hg188308
hg178308
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5215
Supporting Variants
SamplesNA15510
Known Genes
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)nssv11120
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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