A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9945



Internal ID15540035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:110502889..110523866hg38UCSC Ensembl
Outerchr11:110373613..110394590hg19UCSC Ensembl
Outerchr11:109878823..109899800hg18UCSC Ensembl
Outerchr11:109878823..109899800hg17UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg387444
hg197444
hg187444
hg177444
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv485
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)nssv9945
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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