A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561



Internal ID5087114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:75755643..75790599hg19UCSC Ensembl
Outerchr9:74945463..74980419hg18UCSC Ensembl
Outerchr9:72985197..73020153hg17UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg196032
hg186032
hg176032
Variant TypeCNV Insertion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv809
SamplesNA19240
Known GenesANXA1
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)nsv6561
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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