A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10912



Internal ID15539500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:28068438..28099924hg38UCSC Ensembl
Outerchr13:28642575..28674061hg19UCSC Ensembl
Outerchr13:27540575..27572061hg18UCSC Ensembl
Outerchr13:27540575..27572061hg17UCSC Ensembl
Cytoband13q12.2
Allele length
AssemblyAllele length
hg388400
hg198400
hg188400
hg178400
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv973
Supporting Variants
SamplesNA15510
Known GenesFLT3
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)nssv10912
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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