A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1931



Internal ID15541214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:28965778..28995939hg38UCSC Ensembl
Outerchr11:28987325..29017486hg19UCSC Ensembl
Outerchr11:28943901..28974062hg18UCSC Ensembl
Outerchr11:28943901..28974062hg17UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3830162
hg1930162
hg1830162
hg1730162
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7722
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)nssv1931
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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