A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10680



Internal ID15542118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:116579604..116611200hg38UCSC Ensembl
Outerchr9:119341883..119373479hg19UCSC Ensembl
Outerchr9:118381704..118413300hg18UCSC Ensembl
Outerchr9:116421437..116453033hg17UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg387908
hg197908
hg187908
hg177908
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6689
Supporting Variants
SamplesNA18956
Known GenesASTN2
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)nssv10680
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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