A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7676



Internal ID15552709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:10667597..10712592hg38UCSC Ensembl
Outerchr11:10689144..10734139hg19UCSC Ensembl
Outerchr11:10645720..10690715hg18UCSC Ensembl
Outerchr11:10645720..10690715hg17UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg3844996
hg1944996
hg1844996
hg1744996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5350
SamplesNA19129
Known GenesMRVI1
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)nsv7676
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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