A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv436



Internal ID15549061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:93233834..93252508hg38UCSC Ensembl
Outerchr11:92967000..92985674hg19UCSC Ensembl
Outerchr11:92606648..92625322hg18UCSC Ensembl
Outerchr11:92606648..92625322hg17UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3818675
hg1918675
hg1818675
hg1718675
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10832
SamplesNA18956
Known Genes
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)nsv436
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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