A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6457



Internal ID15537407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:47026529..47043563hg38UCSC Ensembl
Outerchr11:47048080..47065114hg19UCSC Ensembl
Outerchr11:47004656..47021690hg18UCSC Ensembl
Outerchr11:47004656..47021690hg17UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3817035
hg1917035
hg1817035
hg1717035
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv312
Supporting Variants
SamplesNA12156
Known GenesC11orf49
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)nssv6457
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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