A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7680



Internal ID15552714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:11674486..11695253hg38UCSC Ensembl
Outerchr11:11696033..11716800hg19UCSC Ensembl
Outerchr11:11652609..11673376hg18UCSC Ensembl
Outerchr11:11652609..11673376hg17UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg3820768
hg1920768
hg1820768
hg1720768
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6448
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)nsv7680
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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