A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv823



Internal ID15544710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:110623515..110655825hg38UCSC Ensembl
Outerchr9:113385795..113418105hg19UCSC Ensembl
Outerchr9:112425616..112457926hg18UCSC Ensembl
Outerchr9:110465350..110497660hg17UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg388692
hg198692
hg188692
hg178692
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6664
Supporting Variants
SamplesNA19240
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)nssv823
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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