A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8855



Internal ID15535009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:122682322..122712172hg38UCSC Ensembl
Outerchr10:124441838..124471688hg19UCSC Ensembl
Outerchr10:124431828..124461678hg18UCSC Ensembl
Outerchr10:124431828..124461678hg17UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg385555
hg195555
hg185555
hg175555
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7584
Supporting Variants
SamplesNA12156
Known GenesC10orf120
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)nssv8855
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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