A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7549



Internal ID5089700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:112840264..112855864hg19UCSC Ensembl
Outerchr10:112830254..112845854hg18UCSC Ensembl
Outerchr10:112830254..112845854hg17UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg195870
hg185870
hg175870
Variant TypeCNV Insertion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv5318
SamplesNA19129
Known GenesADRA2A
Method
AnalysisSample level sites were merged to generate a set of non-redundant variant regions. Two non-redundant inversion variants (chr 2 positions 89438708-89655419 and 89958869-91208466) were corrected from the original publication for coordinates and associated sample-level data.
PlatformCapillary
Comments
ReferenceKidd et al 2008
Pubmed ID18451855
Accession Number(s)nsv7549
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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