A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7721



Internal ID15552759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:28760191..28804851hg38UCSC Ensembl
Outerchr11:28781738..28826398hg19UCSC Ensembl
Outerchr11:28738314..28782974hg18UCSC Ensembl
Outerchr11:28738314..28782974hg17UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3844661
hg1944661
hg1844661
hg1744661
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8892
SamplesNA12156
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)nsv7721
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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