A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7652



Internal ID15552683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:4925015..4976539hg38UCSC Ensembl
Outerchr11:4946245..4997769hg19UCSC Ensembl
Outerchr11:4902821..4954345hg18UCSC Ensembl
Outerchr11:4902821..4954345hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3851525
hg1951525
hg1851525
hg1751525
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6443, nssv10886, nssv1926, nssv10799, nssv3922
SamplesNA12156, NA12878, NA18956, NA15510, NA18555
Known GenesOR51A2, OR51A4
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)nsv7652
Frequency
Sample Size9
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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