A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7677



Internal ID15552710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:11242748..11249423hg38UCSC Ensembl
Outerchr11:11264295..11270970hg19UCSC Ensembl
Outerchr11:11220871..11227546hg18UCSC Ensembl
Outerchr11:11220871..11227546hg17UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg385884
hg195884
hg185884
hg175884
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5351, nssv10804, nssv2858
SamplesNA18956, NA18555, NA19129
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)nsv7677
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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