A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10887



Internal ID15539475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:5760863..5791003hg38UCSC Ensembl
Outerchr11:5782093..5812233hg19UCSC Ensembl
Outerchr11:5738669..5768809hg18UCSC Ensembl
Outerchr11:5738669..5768809hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3830141
hg1930141
hg1830141
hg1730141
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7654
Supporting Variants
SamplesNA15510
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)nssv10887
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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