A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7654



Internal ID15552685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:5760863..5804970hg38UCSC Ensembl
Outerchr11:5782093..5826200hg19UCSC Ensembl
Outerchr11:5738669..5782776hg18UCSC Ensembl
Outerchr11:5738669..5782776hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3844108
hg1944108
hg1844108
hg1744108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10887, nssv5347, nssv9816
SamplesNA18507, NA15510, NA19129
Known GenesOR52N1, OR52N5
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)nsv7654
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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