A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9824



Internal ID15539888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:93936324..93984807hg38UCSC Ensembl
Outerchr11:93669490..93717973hg19UCSC Ensembl
Outerchr11:93309138..93357621hg18UCSC Ensembl
Outerchr11:93309138..93357621hg17UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3848484
hg1948484
hg1848484
hg1748484
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv442
Supporting Variants
SamplesNA18507
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)nssv9824
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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