A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556



Internal ID15203695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:132181602..132226053hg38UCSC Ensembl
Outerchr11:132051496..132095947hg19UCSC Ensembl
Outerchr11:131556706..131601157hg18UCSC Ensembl
Outerchr11:131556706..131601157hg17UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3844452
hg1944452
hg1844452
hg1744452
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8983
SamplesNA12156
Known GenesNTM
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)nsv556
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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