A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5353



Internal ID15543174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:36531197..36545042hg38UCSC Ensembl
Outerchr11:36552747..36566592hg19UCSC Ensembl
Outerchr11:36509323..36523168hg18UCSC Ensembl
Outerchr11:36509323..36523168hg17UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg387039
hg197039
hg187039
hg177039
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7736
Supporting Variants
SamplesNA19129
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)nssv5353
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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