A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3969



Internal ID15538696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:82130920..82163173hg38UCSC Ensembl
Outerchr11:81841962..81874215hg19UCSC Ensembl
Outerchr11:81519610..81551863hg18UCSC Ensembl
Outerchr11:81519610..81551863hg17UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3832254
hg1932254
hg1832254
hg1732254
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv409
Supporting Variants
SamplesNA12878
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)nssv3969
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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