A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10668



Internal ID15195444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:12155307..12187443hg38UCSC Ensembl
Outerchr10:12197306..12229442hg19UCSC Ensembl
Outerchr10:12237312..12269448hg18UCSC Ensembl
Outerchr10:12237312..12269448hg17UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg387366
hg197366
hg187366
hg177366
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5820
Supporting Variants
SamplesNA18956
Known GenesNUDT5, SEC61A2
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)nssv10668
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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