A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1956



Internal ID15541239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:93931951..93964443hg38UCSC Ensembl
Outerchr11:93665117..93697609hg19UCSC Ensembl
Outerchr11:93304765..93337257hg18UCSC Ensembl
Outerchr11:93304765..93337257hg17UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3832493
hg1932493
hg1832493
hg1732493
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv442
Supporting Variants
SamplesNA18555
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)nssv1956
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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