A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv442



Internal ID15549127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:93931951..93984807hg38UCSC Ensembl
Outerchr11:93665117..93717973hg19UCSC Ensembl
Outerchr11:93304765..93357621hg18UCSC Ensembl
Outerchr11:93304765..93357621hg17UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3852857
hg1952857
hg1852857
hg1752857
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1956, nssv9824, nssv8949
SamplesNA18507, NA12156, NA18555
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)nsv442
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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