A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7711



Internal ID15552748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:24310903..24337387hg38UCSC Ensembl
Outerchr11:24332449..24358933hg19UCSC Ensembl
Outerchr11:24289025..24315509hg18UCSC Ensembl
Outerchr11:24289025..24315509hg17UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3826485
hg1926485
hg1826485
hg1726485
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1929
SamplesNA18555
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)nsv7711
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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