A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589



Internal ID15551513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:83407627..83441511hg38UCSC Ensembl
Outerchr9:86022542..86056426hg19UCSC Ensembl
Outerchr9:85212362..85246246hg18UCSC Ensembl
Outerchr9:83252096..83285980hg17UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg385554
hg195554
hg185554
hg175554
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8621
SamplesNA12156
Known GenesFRMD3
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)nsv6589
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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